nifedipine has been researched along with cellulose in 23 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (4.35) | 18.7374 |
| 1990's | 4 (17.39) | 18.2507 |
| 2000's | 12 (52.17) | 29.6817 |
| 2010's | 5 (21.74) | 24.3611 |
| 2020's | 1 (4.35) | 2.80 |
| Authors | Studies |
|---|---|
| Arita, T; Kohri, N; Miyazaki, K; Mori, K | 1 |
| Hirayama, F; Horikawa, T; Uekama, K; Wang, Z | 1 |
| Hirayama, F; Uekama, K; Wang, Z | 1 |
| Ofoefule, SI | 1 |
| Alonso, MJ; Portero, A; Remuñán-López, C; Vila-Jato, JL | 1 |
| Khang, G; Lee, HB; Liu, L; Rhee, JM | 1 |
| Helin-Tanninen, M; Kontra, K; Naaranlahti, T; Wallenius, K | 1 |
| Huang, KK; Meng, CL; Wang, DP | 1 |
| Danjo, K; Hirasawa, N; Ishise, S; Miyata, H | 1 |
| Khang, G; Lee, HB; Liu, LX; Rhee, JM | 1 |
| Bentzley, CM; Huang, J; Schwartz, JB; Wigent, RJ | 1 |
| Helin-Tanninen, M; Kontra, K; Naaranlahti, T; Savolainen, K | 1 |
| Huang, J; Schwartz, JB; Wigent, RJ | 1 |
| Liu, L; Xu, X | 1 |
| Khang, G; Kim, MS; Lee, DH; Lee, HB; Park, JS; Rhee, JM; Shin, JH | 1 |
| Momin, MN; Nokhodchi, A; Rashidi, PA; Shahsavari, M; Shokri, J | 1 |
| Abd El-Sattar Fahmy, S; Ayres, JW; Christensen, JM | 1 |
| Wei, YM; Yu, Y; Zhao, L; Zheng, WW | 1 |
| Huang, J; Li, Y; Malick, WA; Sandhu, HK; Shah, NH; Singhal, D; Wigent, RJ | 1 |
| Dürig, T; Hussain, M; Reed, C; Talukder, R | 1 |
| Cai, C; Cheng, Z; Ma, J; Tang, X; Teng, H; Wang, J; Xu, H; Yin, T | 1 |
| de Villiers, MM; Derdour, L; Huang, J; Hussain, MA; Qian, F; Yu, L; Zhang, SW | 1 |
| Chen, Y; Dong, X; Han, M; Hu, L; Li, G; Liu, Y; Meng, X; Yu, J | 1 |
23 other study(ies) available for nifedipine and cellulose
| Article | Year |
|---|---|
Sustained release of nifedipine from granules.
Topics: Animals; Cellulose; Delayed-Action Preparations; Hydrogen-Ion Concentration; Methylcellulose; Nifedipine; Powders; Rabbits; Time Factors | 1986 |
Design and in-vitro evaluation of a modified-release oral dosage form of nifedipine by hybridization of hydroxypropyl-beta-cyclodextrin and hydroxypropylcellulose.
Topics: 2-Hydroxypropyl-beta-cyclodextrin; beta-Cyclodextrins; Cellulose; Chemistry, Pharmaceutical; Cyclodextrins; Delayed-Action Preparations; Drug Design; Nifedipine; Powders; Solubility; Tablets | 1993 |
In-vivo and in-vitro evaluations of a modified-release oral dosage form of nifedipine by hybridization of hydroxypropyl-beta-cyclodextrin and hydroxypropylcelluloses in dogs.
Topics: 2-Hydroxypropyl-beta-cyclodextrin; Administration, Oral; Animals; beta-Cyclodextrins; Biological Availability; Cellulose; Cyclodextrins; Delayed-Action Preparations; Dogs; Intestinal Absorption; Male; Nifedipine; Technology, Pharmaceutical | 1994 |
Effect of polyethyleneglycol 4000 (PEG4000) solution on the in vitro release profile of nifedipine from polymer matrices.
Topics: Acrylic Resins; Calcium Channel Blockers; Cellulose; Delayed-Action Preparations; Nifedipine; Polyethylene Glycols; Polymethacrylic Acids; Surface-Active Agents; Tablets | 1997 |
Design and evaluation of chitosan/ethylcellulose mucoadhesive bilayered devices for buccal drug delivery.
Topics: Adhesives; Animals; Cattle; Cellulose; Cheek; Chitin; Chitosan; Drug Delivery Systems; Evaluation Studies as Topic; Microscopy, Electron; Nifedipine; Propranolol | 1998 |
Monolithic osmotic tablet system for nifedipine delivery.
Topics: Calcium Channel Blockers; Capsules; Cellulose; Chromatography, High Pressure Liquid; Excipients; Molecular Weight; Multivariate Analysis; Nifedipine; Osmosis; Polyethylene Glycols; Potassium Chloride; Solubility; Tablets | 2000 |
Enteral suspension of nifedipine for neonates. Part 1. Formulation of nifedipine suspension for hospital use.
Topics: Calcium Channel Blockers; Cellulose; Chemistry, Pharmaceutical; Drug Carriers; Drug Combinations; Drug Stability; Humans; Hypromellose Derivatives; Infant, Newborn; Methylcellulose; Nifedipine; Suspensions | 2001 |
Development of extended release dosage forms using non-uniform drug distribution techniques.
Topics: Administration, Oral; Animals; Cellulose; Chemistry, Pharmaceutical; Delayed-Action Preparations; Drug Compounding; Kinetics; Nifedipine; Pharmaceutical Preparations; Rabbits; Solubility; Technology, Pharmaceutical | 2002 |
Physicochemical characterization and drug release studies of nilvadipine solid dispersions using water-insoluble polymer as a carrier.
Topics: Calorimetry, Differential Scanning; Carboxymethylcellulose Sodium; Cellulose; Crystallization; Dosage Forms; Drug Carriers; Microscopy, Electron, Scanning; Nifedipine; Povidone; Solubility; Spectroscopy, Fourier Transform Infrared; Time Factors; X-Ray Diffraction | 2003 |
[Sandwiched osmotic pump tablet for controlled release of water-insoluble drug].
Topics: Cellulose; Delayed-Action Preparations; Drug Carriers; Nifedipine; Osmosis; Polyethylene Glycols; Potassium Chloride; Solubility; Tablets; Technology, Pharmaceutical | 2003 |
Nifedipine solid dispersion in microparticles of ammonio methacrylate copolymer and ethylcellulose binary blend for controlled drug delivery. Effect of drug loading on release kinetics.
Topics: Acrylic Resins; Calcium Channel Blockers; Cellulose; Delayed-Action Preparations; Diffusion; Drug Compounding; Kinetics; Models, Chemical; Nifedipine; Particle Size; Solubility | 2006 |
Nifedipine capsules may provide a viable alternative to oral powders for paediatric patients.
Topics: Calcium Channel Blockers; Capsules; Cellulose; Child; Chromatography, High Pressure Liquid; Drug Compounding; Excipients; Humans; Lactose; Nifedipine; Pharmacopoeias as Topic; Powders; Quality Control | 2007 |
Drug-polymer interaction and its significance on the physical stability of nifedipine amorphous dispersion in microparticles of an ammonio methacrylate copolymer and ethylcellulose binary blend.
Topics: Calcium Channel Blockers; Calorimetry, Differential Scanning; Cellulose; Chemical Phenomena; Chemistry, Pharmaceutical; Chemistry, Physical; Crystallization; Drug Stability; Hydrogen Bonding; Nanoparticles; Nifedipine; Particle Size; Polymers; Spectrophotometry, Infrared; Spectroscopy, Fourier Transform Infrared; X-Ray Diffraction | 2008 |
Preparation of bilayer-core osmotic pump tablet by coating the indented core tablet.
Topics: Calcium Channel Blockers; Carboxymethylcellulose Sodium; Cellulose; Chemistry, Pharmaceutical; Excipients; Kinetics; Membranes, Artificial; Nifedipine; Osmosis; Permeability; Polyethylene Glycols; Povidone; Sodium Chloride; Solubility; Tablets; Technology, Pharmaceutical | 2008 |
A squeeze-type osmotic tablet for controlled delivery of nifedipine.
Topics: Cellulose; Delayed-Action Preparations; Hypromellose Derivatives; Membranes, Artificial; Methylcellulose; Molecular Weight; Nifedipine; Osmosis; Osmotic Pressure; Polyethylene Glycols; Polyvinyl Alcohol; Potassium Chloride; Sodium Chloride; Tablets; Triacetin | 2008 |
Factors affecting the release of nifedipine from a swellable elementary osmotic pump.
Topics: Administration, Oral; Castor Oil; Cellulose; Chemistry, Pharmaceutical; Delayed-Action Preparations; Drug Carriers; Drug Compounding; Gels; Hydrogen-Ion Concentration; Hypromellose Derivatives; Kinetics; Membranes, Artificial; Methylcellulose; Models, Chemical; Nifedipine; Osmosis; Permeability; Plasticizers; Potassium Chloride; Sodium Dodecyl Sulfate; Solubility; Tablets; Water; Wetting Agents | 2008 |
Development of novel spray coated soft elastic gelatin capsule sustained release formulations of nifedipine.
Topics: Calcium Channel Blockers; Capsules; Cellulose; Delayed-Action Preparations; Excipients; Gelatin; Hydrogen-Ion Concentration; Hypromellose Derivatives; Methylcellulose; Nifedipine; Pectins; Polymers; Solubility | 2009 |
Polymer blends used to prepare nifedipine loaded hollow microspheres for a floating-type oral drug delivery system: in vitro evaluation.
Topics: Administration, Oral; Calcium Channel Blockers; Cellulose; Chemistry, Pharmaceutical; Delayed-Action Preparations; Drug Carriers; Drug Compounding; Drug Stability; Ethanol; Ether; Hydrophobic and Hydrophilic Interactions; Kinetics; Microspheres; Models, Chemical; Nifedipine; Particle Size; Povidone; Solubility; Solvents; Surface Properties; Technology, Pharmaceutical | 2010 |
Interplay of formulation and process methodology on the extent of nifedipine molecular dispersion in polymers.
Topics: Calorimetry, Differential Scanning; Cellulose; Chemical Precipitation; Chemistry, Pharmaceutical; Crystallography, X-Ray; Drug Carriers; Drug Compounding; Kinetics; Nifedipine; Polymers; Powder Diffraction; Solubility; Solvents; Spectroscopy, Fourier Transform Infrared; Technology, Pharmaceutical; Transition Temperature | 2011 |
Dissolution and solid-state characterization of poorly water-soluble drugs in the presence of a hydrophilic carrier.
Topics: Calorimetry, Differential Scanning; Carbamazepine; Cellulose; Chemistry, Pharmaceutical; Crystallization; Crystallography, X-Ray; Drug Carriers; Drug Compounding; Hydrophobic and Hydrophilic Interactions; Ibuprofen; Kinetics; Molecular Weight; Nifedipine; Solubility; Technology, Pharmaceutical; Wettability | 2011 |
Sustained-release pellets of nifedipine using microcrystals combined with MCC-based matrix.
Topics: Animals; Biological Availability; Cellulose; Chemistry, Pharmaceutical; Delayed-Action Preparations; Dogs; Drug Stability; Microscopy, Electron, Scanning; Nifedipine; Particle Size; Solubility; Therapeutic Equivalency; Vasodilator Agents | 2015 |
A method to evaluate the effect of contact with excipients on the surface crystallization of amorphous drugs.
Topics: Cellulose; Chemistry, Pharmaceutical; Crystallization; Excipients; Humidity; Indomethacin; Kinetics; Lactose; Mannitol; Nifedipine; Stearic Acids; Surface Properties; Tablets; Technology, Pharmaceutical; Water | 2014 |
Synthesis and characterization of osmotic pump capsules containing polyoxyethylene and pH modifier to control the release of nifedipine.
Topics: Animals; Capsules; Cellulose; Delayed-Action Preparations; Drug Evaluation, Preclinical; Drug Liberation; Excipients; Hydrogen-Ion Concentration; Nifedipine; Osmotic Pressure; Poloxamer; Rabbits; Solubility; Tablets | 2021 |