Page last updated: 2024-11-07

carboxypolymethylene

Description Research Excerpts Clinical Trials Roles Classes Pathways Study Profile Bioassays Related Drugs Related Conditions Protein Interactions Research Growth Market Indicators

Description

carbomer: high molecular polyanionic substance [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID120393
MeSH IDM0049756

Synonyms (17)

Synonym
carbomer
1,3-propanediol, 2-(chloromethyl)-2-((2-naphthalenyloxy)methyl)-
1,3-propanediol, 2-(chloromethyl)-2-((2-naphthyloxy)methyl)-
2-(chloromethyl)-2-((2-naphthyloxy)methyl)-1,3-propanediol
chloromethyl-2 beta-naphthyloxymethyl-2 propanediol-1,3 [french]
brn 2530090
hc 1532
2-(chloromethyl)-2-[(naphthalen-2-yloxy)methyl]propane-1,3-diol
9007-20-9
842-91-1
2-(chloromethyl)-2-(naphthalen-2-yloxymethyl)propane-1,3-diol
chloromethyl-2 beta-naphthyloxymethyl-2 propanediol-1,3
AS-71653
FT-0778246
AKOS037646953
DTXSID60864160
2-(chloromethyl)-2-{[(naphthalen-2-yl)oxy]methyl}propane-1,3-diol

Research Excerpts

Toxicity

ExcerptReferenceRelevance
"The aim of the present study was to determine whether applying obstetric gel, a noninvasive method of pain management that is safe both for the mother and the child, during labor influences delivery satisfaction by facilitating pain management and decreasing exhaustion."( Searching for Medical Substances Safe for Mother and Child, Facilitating the Delivery of Pain Management and Decreasing Exhaustion--Evaluation of Obstetric Gel by Pregnant Women.
Kwasniewska, A; Makara-Studzinska, M; Rolinska, AA; Tomasz, G, 2015
)
0.42

Pharmacokinetics

ExcerptReferenceRelevance
" The PNS concentrations in rat plasma were analyzed by HPLC-MS-MS method and the relative bioavailability and other pharmacokinetic parameters were estimated using Kinetica4."( Pharmacokinetics and correlation between in vitro release and in vivo absorption of bio-adhesive pellets of panax notoginseng saponins.
Li, Y; Zhang, Y; Zhu, CY, 2017
)
0.46

Bioavailability

ExcerptReferenceRelevance
"The bioavailability and onset of action of drugs with high first-pass metabolism can be significantly improved by administration via the sublingual route."( Effect of excipient and processing variables on adhesive properties and release profile of pentoxifylline from mucoadhesive tablets.
Das, NG; Das, SK; Surapaneni, MS, 2006
)
0.33
"8-fold enhancement of absolute bioavailability for LC with FMA intradermal delivery system was observed compared with oral LC administration in vivo study."( Enhanced bioavailability of L-carnitine after painless intradermal delivery vs. oral administration in rats.
Gao, Y; Li, F; Qin, G; Qiu, Y; Wu, Y; Xu, B; Zhang, S, 2011
)
0.37
"Both in vitro and in vivo studies demonstrated that the FMA intradermal delivery system can enhance the delivery and bioavailability of LC."( Enhanced bioavailability of L-carnitine after painless intradermal delivery vs. oral administration in rats.
Gao, Y; Li, F; Qin, G; Qiu, Y; Wu, Y; Xu, B; Zhang, S, 2011
)
0.37
"The developed HP-β-CD-based mucoadhesive system is a viable alternative to conventional eye drops of DXN due to its ability to enhance bioavailability through its longer precorneal residence time and ability to sustain the release of the drug."( Effect of hydroxypropyl-β-cyclodextrin on the ocular bioavailability of dexamethasone from a pH-induced mucoadhesive hydrogel.
Kant, S; Kesavan, K; Pandit, JK; Singh, PN, 2011
)
0.37
"Besides unravelling the polymer synergism, the study helped in developing an optimal once-a-day gastroretentive drug delivery system with improved bioavailability potential exhibiting excellent swelling, floating and bioadhesive characteristics."( Formulation development of gastroretentive tablets of lamivudine using the floating-bioadhesive potential of optimized polymer blends.
Arora, S; Chaturvedi, SC; Garg, B; Kapil, R; Mandsaurwale, R; Singh, B, 2012
)
0.38
" In addition, the in vitro and in vivo mucoadhesion properties as well as the bioavailability of the coated pellets in rats were evaluated by using VAL suspension and core pellets as control preparations."( Enhanced oral bioavailability of novel mucoadhesive pellets containing valsartan prepared by a dry powder-coating technique.
Cao, QR; Cui, JH; Lee, BJ; Liu, Y; Xu, WJ; Yang, M, 2012
)
0.38
" At the concentrations of 20 to 80 microg x mL(-1), the difference of absorption rate constants (K(a)) was not statistically significant."( [Enhancers on the transmembrane transport of chlorogenic acid].
Deng, SQ; Jiang, XH; Ren, J; Wang, LL; Xiao, Y, 2014
)
0.4
" The PNS concentrations in rat plasma were analyzed by HPLC-MS-MS method and the relative bioavailability and other pharmacokinetic parameters were estimated using Kinetica4."( Pharmacokinetics and correlation between in vitro release and in vivo absorption of bio-adhesive pellets of panax notoginseng saponins.
Li, Y; Zhang, Y; Zhu, CY, 2017
)
0.46
"The aim of this study was optimization of buccal piribedil (PR) mucoadhesive tablets to improve its low bioavailability and provide controlled release for the treatment of Parkinson's disease."( Optimization of piribedil mucoadhesive tablets for efficient therapy of Parkinson's disease: physical characterization and ex vivo drug permeation through buccal mucosa.
Barla Demirkoz, A; Çelik, B; Özdemir, S; Üner, M, 2017
)
0.46
"Short residence time, poor bioavailability and poor permeability are the major problems for conventional eye drops treatment."( Formulation and ex vivo-in vivo evaluation of pH-triggered brimonidine tartrate in situ gel for the glaucoma treatment using application of 3
Barse, RK; Kokare, CR; Sharma, JP; Sharma, PK; Tagalpallewar, AA, 2018
)
0.48
"Reduced bioavailability of azelnidipine is related to its poor aqueous solubility and extensive first-pass metabolism, which hinder its efficacy."( Core-in-cup/liquisol dual tackling effect on azelnidipine buccoadhesive tablet micromeritics, in vitro release, and mucoadhesive strength.
Abd El Rehim, RT; El-Gazayerly, ON; El-Helaly, SN; Rashad, AA, 2019
)
0.51
"The conclusions could be drawn that paeonol-loaded liposome in hydrogel was a kind of novel preparation, and its diffusion in vitro had obvious controlled-release characteristics, which further proved that it might improve the bioavailability of paeonol."( Investigation on the Preparation, Characteristics, and Controlled Release Model of Paeonol-Loaded Liposome in Carbomer Hydrogel.
Cheng, Y; Cheng, Z; Liu, Q; Xia, H; Xu, Y, 2020
)
0.56
"This study aims to improve the solubility and bioavailability of daidzein by preparing the β-cyclodextrin-daidzein/PEG_(20000)/Carbomer_(940) nanocrystals."( [Preparation and in vitro property evaluation of β-cyclodextrin-daidzein/PEG_(20000)/Carbomer_(940) nanocrystals].
Chen, LH; Guan, YM; Ye, SH; Zang, ZZ; Zhou, X; Zhu, WF, 2023
)
0.91

Dosage Studied

ExcerptRelevanceReference
" At present, the drug is marketed in tablet, capsule, syrup, cream, and injectable dosage forms."( In vitro and ex vivo permeation studies of chlorpheniramine maleate gels prepared by carbomer derivatives.
Baykara, T; Ozkan, Y; Savaşer, A; Taş, C, 2004
)
0.32
"The primary objective of this study is to investigate the possibility of using Raman spectroscopy as a process analytical technique (PAT) for quality control during manufacturing of topical dosage forms."( The potential of Raman spectroscopy as a process analytical technique during formulations of topical gels and emulsions.
Ackermann, C; Ciotti, S; Islam, MT; Rodríguez-Hornedo, N, 2004
)
0.32
" Raman shifts of typical commercial raw materials used in topical dosage forms were measured to ascertain the potential of this technique for monitoring and analyzing topical products."( The potential of Raman spectroscopy as a process analytical technique during formulations of topical gels and emulsions.
Ackermann, C; Ciotti, S; Islam, MT; Rodríguez-Hornedo, N, 2004
)
0.32
"Rheological properties exert influence on the manufacturing processes, stability and usability of a dosage form as well as the biological availability of an active ingredient."( [Effect of polymer concentration on rheological properties of Carbopol 980 hydrogels containing trimecainium chloride].
Cirbusová, E; Erös, I; Kónya, M; Subová, M; Vitková, Z, 2005
)
0.33
" These types of topical dosage forms could give sustained delivery of drug onto the skin, could tolerate the incorporation of an enhancer, a humectant and an occlusive phase, so they are interesting promises to improve skin absorption of nonsteroidal anti-inflammatory drugs and to prevent side effects associated."( Release study of diclofenac from new carbomer gels.
Bregni, C; Carlucci, A; Chiappetta, D; Faiden, N; García, R; Pasquali, R, 2008
)
0.35
" These powders would be anticipated to deposit predominately in the lower regions of the lung following inhalation and then undergo delayed rather than instantaneous drug release, offering the potential to reduce dosing frequency and improve patient compliance."( Carbomer-modified spray-dried respirable powders for pulmonary delivery of salbutamol sulphate.
Alhusban, FA; Seville, PC, 2009
)
0.35
"Formulation considerations of a new drug delivery system include controlling the site of release of the active ingredient, maintaining drug level for a suitable time and decreasing dosage frequency."( Technological and biopharmaceutical optimization of nystatin release from a multiparticulate based bioadhesive drug delivery system.
Bozó, T; Dévay, A; Kocsis, B; Nagy, S; Pál, S, 2013
)
0.39
" Physicochemical properties, such as moisture, mucoadhesion, thickness, tensile strength, disintegration in phosphate buffer were determined in obtained samples of this dosage form."( Development of Composition and Technologies of Dental Film with Ketorolac Trometamine.
Anurova, MN; Bakhrushina, EO; Demina, NB; Kashperko, AS; Krasnyuk, II; Vakina, MG; Zhilyakova, ET, 2021
)
0.62
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (120)

TimeframeStudies, This Drug (%)All Drugs %
pre-19900 (0.00)18.7374
1990's1 (0.83)18.2507
2000's28 (23.33)29.6817
2010's74 (61.67)24.3611
2020's17 (14.17)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 29.90

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 Index29.90 (24.57)
Research Supply Index4.96 (2.92)
Research Growth Index6.51 (4.65)
Search Engine Demand Index36.71 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (29.90)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials18 (14.52%)5.53%
Reviews2 (1.61%)6.00%
Case Studies2 (1.61%)4.05%
Observational0 (0.00%)0.25%
Other102 (82.26%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]