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sodium pertechnetate tc 99m

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Description

Sodium Pertechnetate Tc 99m: A gamma-emitting radionuclide imaging agent used for the diagnosis of diseases in many tissues, particularly in the gastrointestinal system, cardiovascular and cerebral circulation, brain, thyroid, and joints. [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID23689036
MeSH IDM0021100

Synonyms (46)

Synonym
23288-60-0
sodium pertechnetate 99mtc
technetate (99tco41-), sodium, (t-4)-
sodium pertechnetate tc 99m
99mtco4
unii-a0730cx801
sodium pertechnetate (na(sup 99m)tco4)
pertechnetic acid (h(sup 99m)tco4), sodium salt
sodium pertechnetate tc 99m [usan:usp]
sodium pertechnetate (tc-99m)
tc 99m generator
ultra-technekow fm
a0730cx801 ,
sodium pertechnetium ((sup 99m)tc) injection
pertscan-99m
mpi tc 99m generator
sodium pertechnetate (tc99m)
sodium pertechnetate (99mtc) injection [jan]
sodium pertechnetate tc 99m [usp impurity]
technetium tc 99m sodium pertechnetate [vandf]
sodium pertechnetate component of radiogenix system
sodium pertechnetate tc 99m [usan]
sodium pertechnetate (tc 99m) [vandf]
radiogenix system component sodium pertechnetate
acid (h(sup 99m)tco4), sodium salt
sodium pertechnetate (99m tc) [who-dd]
technetium tc-99m sodium pertechnetate [orange book]
sodium pertechnetate tc 99m [mi]
sodium pertechnetate tc-99m
sodium pertechnetate (99m tc)
pertechnetate (99mtc) sodium
technetium tc-99m sodium pertechnetate
sodium pertechnetate (tc 99m)
sodium pertechnetate (na99mtco4)
pertechnetate sodium tc-99m
DTXSID30177855 ,
MKADDTFVKFMZGF-PUQAOBSFSA-N
Q22075920
Q27273460
sodium;oxido(trioxo)(99tc)technetium-99
sodium pertechnetate tc 99m (usp impurity)
ultra-technekowdte
ultra-technekowv4
dtxcid20225718
technetium tc 99m sodium pertechnetate
ultra-technekow

Research Excerpts

Toxicity

ExcerptReferenceRelevance
" No adverse reactions or side effects were observed."( 99mTc-labeled antihuman epidermal growth factor receptor antibody in patients with tumors of epithelial origin: Part III. Clinical trials safety and diagnostic efficacy.
Borrón, M; Cordero, M; González, J; Gonzalez, N; Iznaga-Escobar, N; Morales, A; Oliva, JP; Perera, A; Pérez, R; Pimentel, G; Ramos-Suzarte, M; Rodríguez, N; Rodríguez, T; Torres, L; Torres, O, 1999
)
0.3

Pharmacokinetics

ExcerptReferenceRelevance
" Anti Xa plasma half-life was 3 times longer for enoxaparin than for heparin."( Pharmacokinetics and biodistribution of technetium 99m labelled standard heparin and a low molecular weight heparin (enoxaparin) after intravenous injection in normal volunteers.
Bara, L; Bok, B; Colas-Linhart, N; Guiraud-Vitaux, F; Imbault, F; Laforest, MD; Marin, J; Samama, M; Uzan, A, 1991
)
0.28
"The pharmacokinetic behavior of pertechnetate in normal subjects has been studied."( Pharmacokinetics of pertechnetate administered after pretreatment with 400 mg of potassium perchlorate: concise communication.
Bancroft, S; Dukstein, WG; Prince, JR, 1980
)
0.26
" The 99mTc method is considered to be a reliable technique for measuring perinatal blood volumes in sheep with the short half-life of the isotope offering additional advantages."( Measurement of blood volume in fetal and neonatal sheep using red blood cells labelled with 99m technetium.
Marker, JD; Scroop, GC; Seamark, RF; Stankewytsch-Janusch, B, 1981
)
0.26
" After administration, blood samples were collected from 7 patients from an antecubital vein opposite to the injection side at intervals from 2 min to 24 hr after injection, and plasma samples were obtained for pharmacokinetic analysis."( Technetium-99m-antiepidermal growth factor-receptor antibody in patients with tumors of epithelial origin: part II. Pharmacokinetics and clearances.
Iznaga-Escobar, N; Morales Morales, A; Pérez Rodríguez, R; Ramos Suzarte, M; Rodríguez Mesa, N; Torres Arocha, LA, 1998
)
0.3
" The pharmacokinetic properties of the 99mTc-labeled anti-EGF-receptor antibody were found to be dose-independent."( Technetium-99m-antiepidermal growth factor-receptor antibody in patients with tumors of epithelial origin: part II. Pharmacokinetics and clearances.
Iznaga-Escobar, N; Morales Morales, A; Pérez Rodríguez, R; Ramos Suzarte, M; Rodríguez Mesa, N; Torres Arocha, LA, 1998
)
0.3
" Clearance from the lung epithelial lining fluid (ELF) of FDKP and insulin have a half-life of ~1 hour."( Insulin lung deposition and clearance following Technosphere® insulin inhalation powder administration.
Amin, N; Baughman, RA; Cassidy, JP; Gotfried, M; Marino, M; Meyer, T; Sommerer, K, 2011
)
0.37
" The terminal clearance half-life from the lung ELF, estimated from sequential BAL fluid measurements for both components, was ~1 hour."( Insulin lung deposition and clearance following Technosphere® insulin inhalation powder administration.
Amin, N; Baughman, RA; Cassidy, JP; Gotfried, M; Marino, M; Meyer, T; Sommerer, K, 2011
)
0.37
" The biodistribution, pharmacokinetic parameters and dopamine concentration was analysed by ultra-HPLC/mass spectrometry method."( Optimised nanoformulation of bromocriptine for direct nose-to-brain delivery: biodistribution, pharmacokinetic and dopamine estimation by ultra-HPLC/mass spectrometry method.
Ali, J; Baboota, S; Fazil, M; Haque, S; Kumar, M; Md, S; Sahni, JK, 2014
)
0.4

Compound-Compound Interactions

ExcerptReferenceRelevance
" ultrasonography (US) of the neck combined with rapid intact parathyroid hormone (iPTH) assay in US-guided fine-needle parathyroid aspirates in preoperative localization of parathyroid adenomas and in directing surgical approach."( Technetium-99m-sestamibi subtraction scintigraphy vs. ultrasonography combined with a rapid parathyroid hormone assay in parathyroid aspirates in preoperative localization of parathyroid adenomas and in directing surgical approach.
Barczynski, M; Buziak-Bereza, M; Cichon, S; Golkowski, F; Hubalewska-Dydejczyk, A; Huszno, B; Konturek, A; Szybinski, Z, 2006
)
0.33
"The results of SS for localization of parathyroid adenoma were determined in 121 patients with primary hyperparathyroidism (pHPT) and compared with findings at surgery and with the results of US alone (in patients without nodular goitre) and US in combination with the iPTH assay in US-guided fine-needle aspirates (FNAs) of suspicious parathyroid lesions (in patients with concomitant nodular goitre)."( Technetium-99m-sestamibi subtraction scintigraphy vs. ultrasonography combined with a rapid parathyroid hormone assay in parathyroid aspirates in preoperative localization of parathyroid adenomas and in directing surgical approach.
Barczynski, M; Buziak-Bereza, M; Cichon, S; Golkowski, F; Hubalewska-Dydejczyk, A; Huszno, B; Konturek, A; Szybinski, Z, 2006
)
0.33
" High-resolution US of the neck was performed by a single endocrine surgeon and combined with US-guided FNAs of suspicious parathyroid lesions in all patients with nodular goitre (n = 43)."( Technetium-99m-sestamibi subtraction scintigraphy vs. ultrasonography combined with a rapid parathyroid hormone assay in parathyroid aspirates in preoperative localization of parathyroid adenomas and in directing surgical approach.
Barczynski, M; Buziak-Bereza, M; Cichon, S; Golkowski, F; Hubalewska-Dydejczyk, A; Huszno, B; Konturek, A; Szybinski, Z, 2006
)
0.33

Bioavailability

ExcerptReferenceRelevance
"To evaluate the interrelationships between the rate of absorption of soluble insulin, SCBF, and anthropometry in normal subjects."( Relationship between absorption of radiolabeled soluble insulin, subcutaneous blood flow, and anthropometry.
Burch, A; Owens, DR; Peters, JR; Vora, JP, 1992
)
0.28
"The rate of absorption of soluble insulin, including during the lag phase, is positively correlated with SCBF."( Relationship between absorption of radiolabeled soluble insulin, subcutaneous blood flow, and anthropometry.
Burch, A; Owens, DR; Peters, JR; Vora, JP, 1992
)
0.28
" These findings indicate that the bioavailability of drugs from controlled release preparations passing through the small intestine is unlikely to be affected by variations in normal daily activity."( Exercise and small intestinal transit.
Hardy, JG; Norman, S; Ollerenshaw, KJ; Wilson, CG, 1987
)
0.27
" The gamma emitter, technitium pertechnetate, enabled estimates of absorption rate to be estimated independently using two approaches."( Modeling of subcutaneous absorption kinetics of infusion solutions in the elderly using technetium.
Campbell, AJ; Lipschitz, S; McQueen, EG; McQueen, M; Roberts, MS; Wanwimolruk, S, 1997
)
0.3
" The mean absorption rate was reduced to 78."( Nuclear scintigraphic assessment of radiation-induced intestinal dysfunction.
Kirichenko, AV; Mason, KA; Rich, TA; Straume, M; Teates, CD, 2000
)
0.31
" The mean absorption rate was reduced to 89 +/- 16% of control in response to a sublethal 4 Gy TBI and dropped to 47."( Nuclear scintigraphic assessment of intestinal dysfunction after combined treatment with 9-amino-20(S)-camptothecin (9-AC) and irradiation.
Kirichenko, AV; Mason, K; Rich, TA; Straume, M; Teates, CD, 2000
)
0.31
" It is generally accepted that a variety of factors other than disease can alter the bioavailability of radiopharmaceuticals and one such factor is the drug therapy."( Assessment of the effect of Punica granatum (pomegranata) on the bioavailability of the radiopharmaceutical sodium pertechnetate (99mTc) in Wistar rats.
Amorim, LF; Bernardo-Filho, M; Brandão, KC; Brito, LM; Catanho, MT; Cavalcanti Jales, RL; De Melo, VG; Gomes, ML; Holanda, CM; Jales-Júnior, LH; Terra, DA, 2003
)
0.32
"To evaluate the effect of a hiperico extract (Hypericum perforatum) on the labeling of blood elements with technetium-99m (99mTc) and in the bioavailability of the radiopharmaceutical sodium pertechnetate in Wistar rats."( [Effect of Hypericum perforatum extract on in vitro labelling of blood elements with technetium-99m and on biodisponibility of sodium pertechnetate in Wistar rats].
Bernardo-Filho, M; Santos-Filho, SD, 2005
)
0.33
"Gastro-retentive dosage forms have the potential to improve local therapy and decrease the variation in bioavailability that is observed with a number of commercially available immediate and modified release preparations."( The use of citric acid to prolong the in vivo gastro-retention of a floating dosage form in the fasted state.
Collett, JH; Fell, JT; Martini, LG; Sharma, HL; Smith, AM; Stops, F, 2006
)
0.33
" The aims of the current study were to: (a) assess the influence of prolonged gastro-retention on the bioavailability of riboflavin from freeze dried calcium alginate beads administered under varying conditions of food intake and (b) to investigate the potential of citric acid to delay the gastric emptying of the calcium alginate beads."( Citric acid prolongs the gastro-retention of a floating dosage form and increases bioavailability of riboflavin in the fasted state.
Collett, JH; Fell, JT; Martini, LG; Sharma, HL; Smith, AM; Stops, F, 2006
)
0.33
" Many substances have been reported to affect the bioavailability of different radiobiocomplexes."( Experimental model to assess possible medicinal herb interaction with a radiobiocomplex: qualitative and quantitative analysis of kidney, liver and duodenum isolated from treated rats.
Bernardo-Filho, M; Caldas, LQ; Carvalho, JJ; Moreno, SR; Nascimento, AL; Olej, B; Pereira, M; Rocha, EK, 2007
)
0.34
"36) on the bioavailability of radio-pharmaceutical 99mTc-sodium pertechnetate (Na99mTcO4) in Wistar rats was investigated."( The effect of "Zusanli" (ST. 36) acupuncture on the bio-availability of sodium pertechnetate in Wistar rats.
Bernardo-Filho, M; França, D; Guimarães, MA; Moreno, SF; Rogers, PA; Santos-Filho, S; Senna-Fernandes, V, 2006
)
0.33
" The aim of this study was to assess the influence of a Nectandra membranacea extract on the bioavailability of the sodium pertechnetate (Na(99m)TcO(4)) radiobiocomplex in rat organs."( The ingestion of a Nectandra membranacea extract changes the bioavailability of technetium-99m radiobiocomplex in rat organs.
Arnobio, A; Bernardo-Filho, M; Caldas, LQ; De Carvalho, JJ; Moreno, SR; Nascimento, L; Olej, B; Oliveira Timoteo, M; Pereira, M; Rocha, EK, 2007
)
0.34
" The aim of this work was to investigate the effects of end-organ response induced by acupuncture point SP6 on the bioavailability of the radiopharmaceutical sodium pertechnetate (Na99mTcO4) in Wistar rats."( Acupuncture stimulation at Sanyinjiao: effect on the sodium pertechnetate bioavailability in rats.
Bernardo-Filho, M; de Almeida, MC; de Carvalho Brito, L; de Souza, DE; de Souza, RS; França, D; Manoel, CV; Senna-Fernandes, V, 2007
)
0.34
"36) by electroacupuncture (EA) at two frequencies on the bioavailability of (99m)Tc-sodium pertechnetate (Na(99m)TcO(4)) in rats."( Effect of Zusanli (ST.36) electroacupuncture at two frequencies on the bioavailability of (99m)Tc-sodium pertechnetate and on labeling of blood constituents in rats.
Bernardo-Filho, M; Cortez, CM; França, DL; Guimarães, MA; Santos, KC; Senna-Fernandes, V; Silva, D; Sousa, RS, 2009
)
0.35
" In the bioavailability analysis, organs and tissues were isolated, their radioactivity determined, and the percentage of injected dose per gram of organ or tissue (%ID/g) and the %ID were calculated for each organ or tissue (%ID/ot)."( Effect of Zusanli (ST.36) electroacupuncture at two frequencies on the bioavailability of (99m)Tc-sodium pertechnetate and on labeling of blood constituents in rats.
Bernardo-Filho, M; Cortez, CM; França, DL; Guimarães, MA; Santos, KC; Senna-Fernandes, V; Silva, D; Sousa, RS, 2009
)
0.35
" The activity over the infusion site was measured using a gamma detector to assess the absorption rate from the SC space."( Absorption rate of subcutaneously infused fluid in ill multimorbid older patients.
Andersen, S; Danielsen, MB; Jødal, L; Jørgensen, MG; Karmisholt, JS; Riis, J; Valdórsson, Ó, 2022
)
0.72
" The absorption rate from the SC space right after the completion of the infusion was 127 ml/h (95% CI 90-164 ml/h)."( Absorption rate of subcutaneously infused fluid in ill multimorbid older patients.
Andersen, S; Danielsen, MB; Jødal, L; Jørgensen, MG; Karmisholt, JS; Riis, J; Valdórsson, Ó, 2022
)
0.72

Dosage Studied

ExcerptRelevanceReference
"Since the minimal effective dosage for radiosynovectomy is not known, we have performed a doubleblind controlled trial of 1 mCi vs."( Radiosynoviorthesis of the knee: a doubleblind trial of 1 versus 5 mCi Gold-198.
Bernelot Moens, HJ; Dijkstra, PF; Hoefnagel, CA; Marcuse, HR; Van Soesbergen, RM, 1988
)
0.27
" A ratio (Rc) of pre- and post-stimulation counts permitted a construction of quantitative dose-response curves; the curve for the parotids had a slight rise of Rc's over 0-20 Gy, whereas that for the submandibular glands had a significant rise over 10-30 Gy; in both glands the rise of Rc's was followed by a steep fall."( Quantitative dose-response analysis of salivary function following radiotherapy using sequential RI-sialography.
Tsujii, H, 1985
)
0.27
" To be a valid quality-control measure, sterility monitoring of prepared radiopharmaceutical dosage forms may need to be performed concurrently with their preparation."( Effect of technetium Tc 99m pertechnetate on bacterial survival in solution.
Coffey, JL; Doerr, GF; Hladik, WB; Miller, CM; Stathis, VJ, 1983
)
0.27
" Dosages were titrated until the patient showed a sitting diastolic blood pressure less than or equal to 90 mm Hg or to a maximum dosage of 100 mg/day of hydrochlorothiazide, 320 mg of propranolol and 20 mg of prazosin."( Monotherapy in mild to moderate hypertension: comparison of hydrochlorothiazide, propranolol and prazosin.
Benowitz, N; Inouye, I; Loge, D; Massie, B; Simpson, P; Topic, N, 1984
)
0.27
"To evaluate the gastric emptying time of pharmaceutical dosage forms in a clinical setting, a relatively simple dual-radionuclide technique was developed."( Gastric emptying of enteric-coated tablets.
Brunelle, RL; Chernish, SM; Hargrove, B; Park, HM; Rosenek, BD; Wellman, HN, 1984
)
0.27
"Factors that influence recommended dosage guidelines for intramuscularly and subcutaneously injected drugs include a spectrum of variables, including therapeutic objective(s), the drug's therapeutic index, the inclusion of concomitant vasoconstrictors, and so on."( Regional blood flow as a determinant of drug absorption description of an animal model.
Karatassas, A; Morris, RG; Orfanos, A, 1993
)
0.29
" Such procedures are undertaken using single infiltration dosage recommendations for lignocaine, both with and without adrenaline."( The relationship between regional blood flow and absorption of lignocaine.
Karatassas, A; Morris, RG; Slavotinek, AH, 1993
)
0.29
"Absence of a maximal dose-response plateau and mathematical modeling suggest that asthmatic airways close during bronchoconstriction."( Airway closure measured by a technegas bolus and SPECT.
Eberl, S; King, GG; Meikle, SR; Salome, CM; Woolcock, AJ, 1997
)
0.3
" Boluses of technetium pertechnetate were given both intravenously and subcutaneously on separate occasions with a multiple dosing regimen using three doses on each occasion."( Modeling of subcutaneous absorption kinetics of infusion solutions in the elderly using technetium.
Campbell, AJ; Lipschitz, S; McQueen, EG; McQueen, M; Roberts, MS; Wanwimolruk, S, 1997
)
0.3
"Gastroretentive dosage forms have potential for use as controlled-release drug delivery systems."( Floating dosage forms: an in vivo study demonstrating prolonged gastric retention.
Collett, JH; Fell, JT; Sharma, HL; Smith, A; Whitehead, L, 1998
)
0.3
" The purpose of this study was to investigate the pharmacokinetics, clearances and possible differences of two dosage administrations of the 99mTc-labeled antiepidermal growth factor (EGF)-receptor antibody and to predict the best dose and schedule for future clinical evaluations of this radiopharmaceutical."( Technetium-99m-antiepidermal growth factor-receptor antibody in patients with tumors of epithelial origin: part II. Pharmacokinetics and clearances.
Iznaga-Escobar, N; Morales Morales, A; Pérez Rodríguez, R; Ramos Suzarte, M; Rodríguez Mesa, N; Torres Arocha, LA, 1998
)
0.3
"The absence of a maximal dose-response plateau as well as gas trapping and increases in closing capacity (CC) suggest that increased airway closure is an important mechanical abnormality of asthmatic airways."( Differences in airway closure between normal and asthmatic subjects measured with single-photon emission computed tomography and technegas.
Eberl, S; King, GG; Salome, CM; Woolcock, AJ; Young, IH, 1998
)
0.3
" A jejunal microcolony assay showed no loss of crypts and hence no measured dose-response effects after 4, 6 or 8 Gy TBI."( Nuclear scintigraphic assessment of radiation-induced intestinal dysfunction.
Kirichenko, AV; Mason, KA; Rich, TA; Straume, M; Teates, CD, 2000
)
0.31
" The pattern of deposition and clearance of the nasal dosage forms were evaluated using a radioactive tracer and the non-invasive technique of gamma scintigraphy."( Clearance characteristics of chitosan based formulations in the sheep nasal cavity.
Davis, SS; Hinchcliffe, M; Illum, L; Soane, RJ, 2001
)
0.31
" In addition, dose-response curves were calculated."( Evaluation of salivary gland function after treatment of head-and-neck tumors with intensity-modulated radiotherapy by quantitative pertechnetate scintigraphy.
Debus, J; Hof, H; Hoffner, SG; Karger, CP; Münter, MW; Nill, S; Rudat, V; Thilmann, C; Wannenmacher, M, 2004
)
0.32
" For the end point of a reduction in the parotid excretion rate of >50% and 75%, the dose-response curves yielded a dose at 50% complication probability of 34."( Evaluation of salivary gland function after treatment of head-and-neck tumors with intensity-modulated radiotherapy by quantitative pertechnetate scintigraphy.
Debus, J; Hof, H; Hoffner, SG; Karger, CP; Münter, MW; Nill, S; Rudat, V; Thilmann, C; Wannenmacher, M, 2004
)
0.32
" At predetermined times after dosing (3, 6, 12, 24 or 32 h), the distribution of radioactivity throughout excised gastrointestinal tracts was determined by gamma scintigraphy."( Gastrointestinal transit in the common brushtail possum measured by gamma scintigraphy.
Davies, NM; McDowell, A; McLeod, BJ; Nicoll, JJ; Tucker, IG, 2005
)
0.33
"Gastro-retentive dosage forms have the potential to improve local therapy and decrease the variation in bioavailability that is observed with a number of commercially available immediate and modified release preparations."( The use of citric acid to prolong the in vivo gastro-retention of a floating dosage form in the fasted state.
Collett, JH; Fell, JT; Martini, LG; Sharma, HL; Smith, AM; Stops, F, 2006
)
0.33
"A floating dosage form based on calcium alginate beads has been developed."( Citric acid prolongs the gastro-retention of a floating dosage form and increases bioavailability of riboflavin in the fasted state.
Collett, JH; Fell, JT; Martini, LG; Sharma, HL; Smith, AM; Stops, F, 2006
)
0.33
" The injury appears as glandular swellings and/or decreased salivation with 131I dosage and passage of time playing significant roles."( False-positive xerostomia following radioactive iodine treatment: case report.
Mandel, L; Mandel, SJ, 2007
)
0.34
" In addition, dose-response curves were calculated."( Changes in salivary gland function after radiotherapy of head and neck tumors measured by quantitative pertechnetate scintigraphy: comparison of intensity-modulated radiotherapy and conventional radiation therapy with and without Amifostine.
Debus, J; Haberkorn, U; Herfarth, KK; Hof, H; Hoffner, S; Huber, P; Karger, CP; Münter, MW; Rudat, V, 2007
)
0.34
" In regard to the endpoint "reduction of the salivary gland excretion rate of more than 50%," the dose-response curves yielded D50-values of 34."( Changes in salivary gland function after radiotherapy of head and neck tumors measured by quantitative pertechnetate scintigraphy: comparison of intensity-modulated radiotherapy and conventional radiation therapy with and without Amifostine.
Debus, J; Haberkorn, U; Herfarth, KK; Hof, H; Hoffner, S; Huber, P; Karger, CP; Münter, MW; Rudat, V, 2007
)
0.34
" Imaging could provide a mechanism to assess DR5 modulation when DR5 therapy is combined with chemotherapy and radiation, and thereby aid in optimizing the dosing schedule."( High-resolution single-photon emission computed tomography and X-ray computed tomography imaging of Tc-99m-labeled anti-DR5 antibody in breast tumor xenografts.
Buchsbaum, DJ; Chaudhuri, TR; Kim, H; Wang, D; Zinn, KR, 2007
)
0.34
" Although the products are labeled to be taken in the erect position, the semisupine position was included to simulate dosing in bedridden patients."( Esophageal transit and in vivo disintegration of branded risedronate sodium tablets and two generic formulations of alendronic acid tablets: a single-center, single-blind, six-period crossover study in healthy female subjects.
Atherton, CT; Blackshaw, PE; Dansereau, RJ; Hay, PD; Lawes, SC; Perkins, AC; Schnell, DJ; Spiller, RC; Wagner, LK, 2008
)
0.35
"There was a significant dose-response relationship between mean parotid dose and functional recuperation."( Longitudinal assessment of parotid function in patients receiving tomotherapy for head-and-neck cancer.
Baron, I; Everaert, H; Storme, G; Tournel, K; Van Esch, G; Vanhove, C; Verellen, D; Voordeckers, M, 2008
)
0.35
" In a single-center, randomized, parallel-group, double-blind, placebo-controlled, dose-response study, we evaluated safety, pharmacodynamics, and pharmacokinetics in female patients with IBS-C."( Effect of a glucagon-like peptide 1 analog, ROSE-010, on GI motor functions in female patients with constipation-predominant irritable bowel syndrome.
Boldingh, A; Burton, D; Camilleri, M; Iturrino, J; Kenny, E; Månsson, M; McKinzie, S; Rao, AS; Vazquez-Roque, M; Wong, BS; Zinsmeister, AR, 2012
)
0.38
"To estimate dose-response relationship using dynamic quantitative (99m)Tc-pertechnate scintigraphy in head-neck cancer patients treated with parotid-sparing conformal radiotherapy."( Prospective longitudinal assessment of parotid gland function using dynamic quantitative pertechnate scintigraphy and estimation of dose-response relationship of parotid-sparing radiotherapy in head-neck cancers.
Agarwal, JP; Budrukkar, A; Ghosh-Laskar, S; Gupta, T; Hotwani, C; Kannan, S; Master, Z; Murthy, V; Rangarajan, V, 2015
)
0.42
" Dose-response curves were modeled using standardized methodology to calculate tolerance dose 50 (TD50) for parotid glands."( Prospective longitudinal assessment of parotid gland function using dynamic quantitative pertechnate scintigraphy and estimation of dose-response relationship of parotid-sparing radiotherapy in head-neck cancers.
Agarwal, JP; Budrukkar, A; Ghosh-Laskar, S; Gupta, T; Hotwani, C; Kannan, S; Master, Z; Murthy, V; Rangarajan, V, 2015
)
0.42
"Patients were divided into five groups on the basis of the cumulative I-131 dosage received."( Systematic evaluation of salivary gland damage following I-131 therapy in differentiated thyroid cancer patients by quantitative scintigraphy and clinical follow-up.
Chen, P; Feng, HJ; Huang, LH; Ouyang, W; Sun, YG; Wang, J; Wu, JQ; Xian, JL, 2015
)
0.42
" A cumulative dosage of greater than 600 mCi resulted in complete loss of %SR in the parotid glands."( Systematic evaluation of salivary gland damage following I-131 therapy in differentiated thyroid cancer patients by quantitative scintigraphy and clinical follow-up.
Chen, P; Feng, HJ; Huang, LH; Ouyang, W; Sun, YG; Wang, J; Wu, JQ; Xian, JL, 2015
)
0.42
" Nevertheless, more consideration should be placed on careful dosing of I-131."( Systematic evaluation of salivary gland damage following I-131 therapy in differentiated thyroid cancer patients by quantitative scintigraphy and clinical follow-up.
Chen, P; Feng, HJ; Huang, LH; Ouyang, W; Sun, YG; Wang, J; Wu, JQ; Xian, JL, 2015
)
0.42
" Subsequently, the patients were given an oral dosage of 3700 MBq 131 I for remnant ablation, and posttreatment whole body scan was performed on day 5 after ablation."( Combined use of radioiodine therapy and radiofrequency ablation in treating postsurgical thyroid remnant of differentiated thyroid carcinoma.
Chen, S; Li, L; Long, B; Wu, P; Xu, D; Yao, L; Ye, X; Yi, H, 2015
)
0.42
" (b) The nearly 100% PPV of Tc-99m imaging immediately before I-131 Tx for remnant detection suggests that Tc-99m imaging not only serves as an alternative to low-dose I-131 scanning in the low-risk post-thyroidectomy patients but also provides a clue for the subsequent I-131 therapeutic dosage and even for the outcome prediction."( Tc-99m imaging in thyroidectomized differentiated thyroid cancer patients immediately before I-131 treatment.
Chang, MC; Cheng, CY; Huang, WS; Kuo, SJ; Lee, CH; Shen, DH; Tsai, CJ; Wang, JJ; Wang, LY, 2016
)
0.43
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (2,994)

TimeframeStudies, This Drug (%)All Drugs %
pre-19901211 (40.45)18.7374
1990's888 (29.66)18.2507
2000's546 (18.24)29.6817
2010's300 (10.02)24.3611
2020's49 (1.64)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 31.42

According to the monthly volume, diversity, and competition of internet searches for this compound, as well the volume and growth of publications, there is estimated to be moderate demand-to-supply ratio for research on this compound.

MetricThis Compound (vs All)
Research Demand Index31.42 (24.57)
Research Supply Index8.13 (2.92)
Research Growth Index4.29 (4.65)
Search Engine Demand Index45.47 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (31.42)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials157 (4.83%)5.53%
Reviews117 (3.60%)6.00%
Case Studies800 (24.61%)4.05%
Observational3 (0.09%)0.25%
Other2,174 (66.87%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Clinical Trials (7)

Trial Overview

TrialPhaseEnrollmentStudy TypeStart DateStatus
Diagnosis of Coronary Artery Disease With Rubidium-82 PET and Technetium-99m-MIBI SPET: A Head to Head Comparison, Versus Coronary CT Angiography [NCT01379677]Phase 3135 participants (Actual)Interventional2011-02-28Completed
Sentinel Lymph Node Biopsy After Nipple Sparing Mastectomy: Prospective Study [NCT04140188]20 participants (Anticipated)Interventional2019-11-30Not yet recruiting
The Prognostic Value of Post Thyroidectomy 99mTCpertechnetate Thyroid Scan in Patient With Differentiated Thyroid Cancer [NCT04563780]113 participants (Anticipated)Observational2020-10-01Recruiting
A Cross-over Comparison of the Diagnostic Accuracy of Technetium (99mTc) Medronate Injection Prepared With 99mTc Derived From Neutron-activation Produced 99Mo Versus the Current Reference Standard of 99mTc Derived From Fission-produced 99Mo [NCT03002454]Phase 34 participants (Actual)Interventional2016-08-31Terminated(stopped due to Altered biodistribution in investigational images versus standard images.)
Inhalation Low Dose Radionuclide Therapy in Comprehensive Treatment of COVID-19 Viral Pneumonia [NCT04724538]Phase 1/Phase 225 participants (Actual)Interventional2020-10-15Completed
Phase I Trial of Intravenous Administration of Vesicular Stomatitis Virus Genetically Engineered to Express Thyroidal Sodium Iodide Symporter (NIS) and Human Interferon Beta (hIFNb), in Patients With Metastatic or Recurrent Endometrial Cancer [NCT03120624]Phase 177 participants (Anticipated)Interventional2017-09-15Recruiting
Simplification of Low Level Internal Dosimetry [NCT03580161]12 participants (Actual)Observational2018-06-30Completed
[information is prepared from clinicaltrials.gov, extracted Sep-2024]

Trial Outcomes

TrialOutcome
NCT03002454 (1) [back to overview]Number of Participants Analyzed for Diagnostic Efficacy of Technetium (99mTc) Medronate Injection Prepared With 99mTc Derived From Neutron-activation Produced 99Mo Imaging Sensitivity Versus 99mTc Derived From Fission-produced 99Mo Imaging Sensitivity.
NCT04724538 (10) [back to overview]Absolute Lymphocyte Count (ALC) After 99mTc-pertechnetate Aerosol Inhalation for Adverse Events Monitoring as Evaluation Safety of This Procedure in Patients With COVID-19 Viral Pneumonia.
NCT04724538 (10) [back to overview]Absolute Neutrophil Count (ANC) After 99mTc-pertechnetate Aerosol Inhalation for Adverse Events Monitoring as Evaluation Safety of This Procedure in Patients With COVID-19 Viral Pneumonia.
NCT04724538 (10) [back to overview]Count of Red Blood Cells (RBC) After 99mTc-pertechnetate Aerosol Inhalation for Adverse Events Monitoring as Evaluation Safety of This Procedure in Patients With COVID-19 Viral Pneumonia.
NCT04724538 (10) [back to overview]Count of White Blood Cells (WBC) After 99mTc-pertechnetate Aerosol Inhalation for Adverse Events Monitoring as Evaluation Safety of This Procedure in Patients With COVID-19 Viral Pneumonia.
NCT04724538 (10) [back to overview]Hemoglobin Count (Hb) After 99mTc-pertechnetate Aerosol Inhalation for Adverse Events Monitoring as Evaluation Safety of This Procedure in Patients With COVID-19 Viral Pneumonia.
NCT04724538 (10) [back to overview]Level of CD4+ T-cells in Blood After 99mTc-pertechnetate Aerosol Inhalation for Evaluation of Cellular Immune Response After This Procedure in Patients With COVID-19 Viral Pneumonia
NCT04724538 (10) [back to overview]Level of D-dimer in Blood After 99mTc-pertechnetate Aerosol Inhalation for Adverse Events Monitoring as Evaluation Safety of This Procedure in Patients With COVID-19 Viral Pneumonia.
NCT04724538 (10) [back to overview]Level of Lactate in the Blood After 99mTc-pertechnetate Aerosol Inhalation for Adverse Events Monitoring as Evaluation Safety of This Procedure in Patients With COVID-19 Viral Pneumonia.
NCT04724538 (10) [back to overview]Level of NK-cells in Blood After 99mTc-pertechnetate Aerosol Inhalation for Evaluation of Cellular Immune Response After This Procedure in Patients With COVID-19 Viral Pneumonia
NCT04724538 (10) [back to overview]Percentage of Neutrophils (N) After 99mTc-pertechnetate Aerosol Inhalation for Adverse Events Monitoring as Evaluation Safety of This Procedure in Patients With COVID-19 Viral Pneumonia.

Number of Participants Analyzed for Diagnostic Efficacy of Technetium (99mTc) Medronate Injection Prepared With 99mTc Derived From Neutron-activation Produced 99Mo Imaging Sensitivity Versus 99mTc Derived From Fission-produced 99Mo Imaging Sensitivity.

All enrolled patients were re-imaged 3 to 28 days post a standard of care fission derived 99Mo bone scan using neutron-activation produced 99Mo as the investigational product. Per protocol dosage, time factors, injection site and imaging camera were matched. Resulting image sets (fission and neutron-activation) were analyzed visually for concordant biodistribution. (NCT03002454)
Timeframe: 60 days

InterventionParticipants (Count of Participants)
99mTc MDP Injection:Neutron-bombardment4

[back to top]

Absolute Lymphocyte Count (ALC) After 99mTc-pertechnetate Aerosol Inhalation for Adverse Events Monitoring as Evaluation Safety of This Procedure in Patients With COVID-19 Viral Pneumonia.

Patients with COVID-19 viral pneumonia were observed for safety after administration of 99mTc-pertechnetate aerosol inhalation, and followed up at 1, 3, 7 days after inhalation. Patients did blood test to observe for abnormalities in clinical parameters and compare to baseline results as assessed by CTCAE v5.0. These tests were also performed in patients with COVID-19 viral pneumonia receiving standard treatment. The results were compared between the two groups. (NCT04724538)
Timeframe: Days 1, 3 and 7 after inhalation

,
Interventionx 1000 cells/microL (Mean)
ALC - 1st dayALC - 3rd dayALC - 7th day
Patient With COVID-19 Pneumonia1.62.11.64
Patient With COVID-19 Pneumonia Without Intervention1.61.41.73

[back to top]

Absolute Neutrophil Count (ANC) After 99mTc-pertechnetate Aerosol Inhalation for Adverse Events Monitoring as Evaluation Safety of This Procedure in Patients With COVID-19 Viral Pneumonia.

Patients with COVID-19 viral pneumonia were observed for safety after administration of 99mTc-pertechnetate aerosol inhalation, and followed up at 1, 3, 7 days after inhalation. Patients did blood test to observe for abnormalities in clinical parameters and compare to baseline results as assessed by CTCAE v5.0. These tests were also performed in patients with COVID-19 viral pneumonia receiving standard treatment. The results were compared between the two groups. (NCT04724538)
Timeframe: Days 1, 3 and 7 after inhalation

,
Interventionx 1000 cells/microL (Mean)
ANC - 1st dayANC - 3rd dayANC - 7th day
Patient With COVID-19 Pneumonia8.86.86.2
Patient With COVID-19 Pneumonia Without Intervention7.46.66.9

[back to top]

Count of Red Blood Cells (RBC) After 99mTc-pertechnetate Aerosol Inhalation for Adverse Events Monitoring as Evaluation Safety of This Procedure in Patients With COVID-19 Viral Pneumonia.

Patients with COVID-19 viral pneumonia were observed for safety after administration of 99mTc-pertechnetate aerosol inhalation, and followed up at 1, 3, 7 days after inhalation. Patients did blood test to observe for abnormalities in clinical parameters and compare to baseline results as assessed by CTCAE v5.0. These tests were also performed in patients with COVID-19 viral pneumonia receiving standard treatment. The results were compared between the two groups. (NCT04724538)
Timeframe: Days 1, 3 and 7 after inhalation

,
Interventionx million cells/microL (Mean)
RBC - 1st dayRBC - 3rd dayRBC - 7th day
Patient With COVID-19 Pneumonia4.54.34.2
Patient With COVID-19 Pneumonia Without Intervention4.54.44.4

[back to top]

Count of White Blood Cells (WBC) After 99mTc-pertechnetate Aerosol Inhalation for Adverse Events Monitoring as Evaluation Safety of This Procedure in Patients With COVID-19 Viral Pneumonia.

Patients with COVID-19 viral pneumonia were observed for safety after administration of 99mTc-pertechnetate aerosol inhalation, and followed up at 1, 3, 7 days after inhalation. Patients did blood test to observe for abnormalities in clinical parameters and compare to baseline results as assessed by CTCAE v5.0. These tests were also performed in patients with COVID-19 viral pneumonia receiving standard treatment. The results were compared between the two groups. (NCT04724538)
Timeframe: Days 1, 3 and 7 after inhalation

,
Interventionx 1000 cells/microL (Mean)
WBC - 1st dayWBC - 3rd dayWBC - 7th day
Patient With COVID-19 Pneumonia11.29.78.8
Patient With COVID-19 Pneumonia Without Intervention9.88.79.3

[back to top]

Hemoglobin Count (Hb) After 99mTc-pertechnetate Aerosol Inhalation for Adverse Events Monitoring as Evaluation Safety of This Procedure in Patients With COVID-19 Viral Pneumonia.

Patients with COVID-19 viral pneumonia were observed for safety after administration of 99mTc-pertechnetate aerosol inhalation, and followed up at 1, 3, 7 days after inhalation. Patients did blood test to observe for abnormalities in clinical parameters and compare to baseline results as assessed by CTCAE v5.0. These tests were also performed in patients with COVID-19 viral pneumonia receiving standard treatment. The results were compared between the two groups. (NCT04724538)
Timeframe: Days 1, 3 and 7 after inhalation

,
Interventiongm/L (Mean)
Hb - 1st dayHb - 3rd dayHb - 7th day
Patient With COVID-19 Pneumonia140.5137.5135.3
Patient With COVID-19 Pneumonia Without Intervention132130.6131

[back to top]

Level of CD4+ T-cells in Blood After 99mTc-pertechnetate Aerosol Inhalation for Evaluation of Cellular Immune Response After This Procedure in Patients With COVID-19 Viral Pneumonia

Patients with COVID-19 viral pneumonia were observed for safety after administration of 99mTc-pertechnetate aerosol inhalation, and followed up at 1, 3, 7 days after inhalation. Patients did blood test to observe for abnormalities in clinical parameters and compare to baseline results as assessed by CTCAE v5.0. These tests were also performed in patients with COVID-19 viral pneumonia receiving standard treatment. The results were compared between the two groups. (NCT04724538)
Timeframe: Days 1, 3 and 7 after inhalation

,
Interventionx 1000 cells/microL (Mean)
CD4 - 1st dayCD4 - 3rd dayCD4 - 7th day
Patient With COVID-19 Pneumonia7611100845
Patient With COVID-19 Pneumonia Without Intervention614832718

[back to top]

Level of D-dimer in Blood After 99mTc-pertechnetate Aerosol Inhalation for Adverse Events Monitoring as Evaluation Safety of This Procedure in Patients With COVID-19 Viral Pneumonia.

Patients with COVID-19 viral pneumonia were observed for safety after administration of 99mTc-pertechnetate aerosol inhalation, and followed up at 1, 3, 7 days after inhalation. Patients did blood test to observe for abnormalities in clinical parameters and compare to baseline results as assessed by CTCAE v5.0. These tests were also performed in patients with COVID-19 viral pneumonia receiving standard treatment. The results were compared between the two groups. (NCT04724538)
Timeframe: Days 1, 3 and 7 after inhalation

,
Interventionngm/mL (Mean)
D-dimer - 1st dayD-dimer - 3rd dayD-dimer - 7th day
Patient With COVID-19 Pneumonia1737843383
Patient With COVID-19 Pneumonia Without Intervention1284685859

[back to top]

Level of Lactate in the Blood After 99mTc-pertechnetate Aerosol Inhalation for Adverse Events Monitoring as Evaluation Safety of This Procedure in Patients With COVID-19 Viral Pneumonia.

Patients with COVID-19 viral pneumonia were observed for safety after administration of 99mTc-pertechnetate aerosol inhalation, and followed up at 1, 3, 7 days after inhalation. Patients did blood test to observe for abnormalities in clinical parameters and compare to baseline results as assessed by CTCAE v5.0. These tests were also performed in patients with COVID-19 viral pneumonia receiving standard treatment. The results were compared between the two groups. (NCT04724538)
Timeframe: Days 1, 3 and 7 after inhalation

,
Interventionmmol/L (Mean)
Lactate - 1st dayLactate - 3rd dayLactate - 7th day
Patient With COVID-19 Pneumonia54.44.28
Patient With COVID-19 Pneumonia Without Intervention4.114.64.81

[back to top]

Level of NK-cells in Blood After 99mTc-pertechnetate Aerosol Inhalation for Evaluation of Cellular Immune Response After This Procedure in Patients With COVID-19 Viral Pneumonia

Patients with COVID-19 viral pneumonia were observed for safety after administration of 99mTc-pertechnetate aerosol inhalation, and followed up at 1, 3, 7 days after inhalation. Patients did blood test to observe for abnormalities in clinical parameters and compare to baseline results as assessed by CTCAE v5.0. These tests were also performed in patients with COVID-19 viral pneumonia receiving standard treatment. The results were compared between the two groups. (NCT04724538)
Timeframe: Days 1, 3 and 7 after inhalation

,
Interventionx 1000 cells/microL (Mean)
NK - 1st dayNK - 3rd dayNK - 7th day
Patient With COVID-19 Pneumonia153188219
Patient With COVID-19 Pneumonia Without Intervention164149181

[back to top]

Percentage of Neutrophils (N) After 99mTc-pertechnetate Aerosol Inhalation for Adverse Events Monitoring as Evaluation Safety of This Procedure in Patients With COVID-19 Viral Pneumonia.

Patients with COVID-19 viral pneumonia were observed for safety after administration of 99mTc-pertechnetate aerosol inhalation, and followed up at 1, 3, 7 days after inhalation. Patients did blood test to observe for abnormalities in clinical parameters and compare to baseline results as assessed by CTCAE v5.0. These tests were also performed in patients with COVID-19 viral pneumonia receiving standard treatment. The results were compared between the two groups. (NCT04724538)
Timeframe: Days 1, 3 and 7 after inhalation

,
Interventionpercentage (Mean)
Percentage of Neutrophils - 1st dayPercentage of Neutrophils - 3rd dayPercentage of Neutrophils - 7th day
Patient With COVID-19 Pneumonia76.368.868.4
Patient With COVID-19 Pneumonia Without Intervention72.272.271.5

[back to top]