verapamil has been researched along with methylcellulose in 15 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 1 (6.67) | 18.2507 |
| 2000's | 11 (73.33) | 29.6817 |
| 2010's | 3 (20.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Aihara, M; Blume, KG; Chao, NJ; Sikic, BI | 1 |
| Bodmeier, R; Dashevsky, A; Siepmann, J; Streubel, A | 1 |
| Baluom, M; Friedman, M; Rubinstein, A | 1 |
| Munday, DL | 1 |
| Bodmeier, R; Pearnchob, N; Siepmann, J | 1 |
| Fassihi, R; Yang, L | 1 |
| Chen, HX; Chen, XJ; Chen, ZP; Li, LR; Xiao, YY; Zhu, JB | 1 |
| Benita, S; Nassar, T; Nyska, A; Rom, A | 1 |
| Caraballo, I; Gonçalves-Araújo, T; Rajabi-Siahboomi, AR | 2 |
| Li, CJ; Yu, WY; Zhu, JB | 1 |
| Modasiya, M; Patel, A; Patel, V; Shah, D | 1 |
| Chakraborty, S; Khandai, M; Patra, ChN; Patro, VJ; Sen, KK; Sharma, A | 1 |
| Baviskar, D; Jain, D; Sharma, R | 1 |
| Doležel, P; Dvořáčková, K; Kejdušová, M; Mašková, E; Muselík, J; Vetchý, D | 1 |
15 other study(ies) available for verapamil and methylcellulose
| Article | Year |
|---|---|
Assessment of purging with multidrug resistance (MDR) modulators and VP-16: results of long-term marrow culture.
Topics: Bone Marrow Cells; Cell Count; Cell Survival; Cells, Cultured; Cyclosporins; Drug Resistance; Etoposide; Granulocytes; Hematopoietic Stem Cells; Humans; Macrophages; Methylcellulose; Verapamil | 1990 |
pH-independent release of a weakly basic drug from water-insoluble and -soluble matrix tablets.
Topics: Calcium Channel Blockers; Delayed-Action Preparations; Excipients; Hydrogen-Ion Concentration; Methylcellulose; Solubility; Tablets; Verapamil; Water | 2000 |
Improved intestinal absorption of sulpiride in rats with synchronized oral delivery systems.
Topics: Administration, Oral; Animals; ATP Binding Cassette Transporter, Subfamily B, Member 1; Intestinal Absorption; Lactose; Methylcellulose; Oxazines; Quinidine; Rats; Sulpiride; Verapamil | 2001 |
Film coated pellets containing verapamil hydrochloride: enhanced dissolution into neutral medium.
Topics: Acrylic Resins; Drug Compounding; Drug Implants; Excipients; Fumarates; Hydrogen-Ion Concentration; Kinetics; Methylcellulose; Microscopy, Electron, Scanning; Solubility; Surface Properties; Time Factors; Verapamil | 2003 |
Pharmaceutical applications of shellac: moisture-protective and taste-masking coatings and extended-release matrix tablets.
Topics: Acetaminophen; Aspirin; Delayed-Action Preparations; Drug Stability; Humans; Hypromellose Derivatives; Methylcellulose; Resins, Plant; Solubility; Taste; Theophylline; Verapamil; Wettability | 2003 |
Accessibility of solid core tablet for dissolution in an asymmetric triple-layer matrix system.
Topics: Administration, Oral; Calcium Channel Blockers; Chemistry, Pharmaceutical; Delayed-Action Preparations; Diffusion; Hypromellose Derivatives; Kinetics; Methylcellulose; Molecular Weight; Polyethylene Glycols; Protease Inhibitors; Solubility; Tablets; Verapamil | 2003 |
[Preparation of verapamil hydrochloride controlled-onset extended-release pellets and its pharmacokinetics in dogs].
Topics: Administration, Oral; Animals; Biological Availability; Calcium Channel Blockers; Cellulose; Delayed-Action Preparations; Dogs; Drug Stability; Hypromellose Derivatives; Methylcellulose; Microscopy, Electron, Scanning; Verapamil | 2006 |
A novel nanocapsule delivery system to overcome intestinal degradation and drug transport limited absorption of P-glycoprotein substrate drugs.
Topics: Animals; ATP Binding Cassette Transporter, Subfamily B; ATP Binding Cassette Transporter, Subfamily B, Member 1; Caco-2 Cells; Chemistry, Pharmaceutical; Cytochrome P-450 CYP3A; Cytochrome P-450 Enzyme System; Drug Carriers; Drug Compounding; Drug Stability; Enterocytes; Humans; Hypromellose Derivatives; In Vitro Techniques; Intestinal Absorption; Intestinal Secretions; Jejunum; Methylcellulose; Microspheres; Nanocapsules; Oils; Polymethacrylic Acids; Rats; Rats, Sprague-Dawley; Solubility; Tacrolimus; Technology, Pharmaceutical; Time Factors; Verapamil | 2008 |
Application of percolation theory in the study of an extended release Verapamil hydrochloride formulation.
Topics: Chemistry, Pharmaceutical; Delayed-Action Preparations; Drug Carriers; Excipients; Hypromellose Derivatives; Methylcellulose; Porosity; Tablets; Verapamil; Viscosity | 2008 |
[Preparation of verapamil hydrochloride core-in-cup tablets with double-pulsatile and multi-phasic release].
Topics: Delayed-Action Preparations; Drug Carriers; Drug Compounding; Drug Delivery Systems; Excipients; Hypromellose Derivatives; Methylcellulose; Tablets; Verapamil | 2008 |
Development and in vivo floating behavior of verapamil HCl intragastric floating tablets.
Topics: Acrylates; Acrylic Resins; Administration, Oral; Animals; Calcium Channel Blockers; Chemistry, Pharmaceutical; Citric Acid; Delayed-Action Preparations; Dogs; Drug Compounding; Drug Stability; Gastric Mucosa; Gels; Humidity; Hypromellose Derivatives; Linear Models; Male; Methylcellulose; Models, Chemical; Polysaccharides, Bacterial; Radiography; Sodium Bicarbonate; Solubility; Stomach; Tablets; Temperature; Verapamil | 2009 |
Effects of drug solubility on the release kinetics of water soluble and insoluble drugs from HPMC based matrix formulations.
Topics: Chemistry, Pharmaceutical; Delayed-Action Preparations; Diclofenac; Hypromellose Derivatives; Methylcellulose; Solubility; Tablets; Verapamil; Water | 2009 |
Polymer percolation threshold in HPMC extended release formulation of carbamazepine and verapamil HCl.
Topics: Analgesics, Non-Narcotic; Anti-Arrhythmia Agents; Carbamazepine; Combinatorial Chemistry Techniques; Computer Simulation; Data Interpretation, Statistical; Delayed-Action Preparations; Diffusion; Drug Combinations; Drug Design; Lactose; Methylcellulose; Models, Chemical; Models, Statistical; Polymers; Verapamil | 2010 |
Modulation of drug release by utilizing pH-independent matrix system comprising water soluble drug verapamil hydrochloride.
Topics: Administration, Oral; Adult; Biological Availability; Calcium Channel Blockers; Calorimetry, Differential Scanning; Chemistry, Pharmaceutical; Delayed-Action Preparations; Diffusion; Drug Carriers; Drug Stability; Humans; Hydrogen-Ion Concentration; Hydrophobic and Hydrophilic Interactions; Hypromellose Derivatives; Kinetics; Male; Methylcellulose; Models, Chemical; Polymers; Polymethacrylic Acids; Povidone; Solubility; Spectroscopy, Fourier Transform Infrared; Tablets; Technology, Pharmaceutical; Verapamil; Water; X-Ray Diffraction; Young Adult | 2013 |
The effect of acid pH modifiers on the release characteristics of weakly basic drug from hydrophlilic-lipophilic matrices.
Topics: Algorithms; Calcium Channel Blockers; Drug Design; Electrodes; Factor Analysis, Statistical; Gels; Hydrogen-Ion Concentration; Hypromellose Derivatives; Kinetics; Methylcellulose; Particle Size; Pharmaceutical Preparations; Solubility; Tablets; Verapamil | 2013 |