in-vitro release study
DEVELOPMENT, CHARACTERIZATION AND IN VITRO ANTIFUNGAL EVALUATION OF PLANTEROSOMAL GEL OF GANODERMA LUCIDUM
... in-vitro release study and ex-vivo permeation study indicate that planterosomal gel release the active constituents from the formulation in a controlled manner, retard the ...
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Application of solvent injection method to develop stable, sustained release solid lipid Nanoparticles of Curcumin
... this study an alternative production method called Solvent Injection Method (SIM) was used to prepare SLNs containing curcumin ...in-vitro release study as well as the stability study ...
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DESIGN AND IN VITRO EVALUATION OF SUSTAINED RELEASE TABLETS OF RANOLAZINE
... in vitro release of Ranolazine SR tablets was studied in 900 ml of ...better release of 99.78±0.99% after 24 hours. It showed Zero-order release with linearity ...in vitro ...
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Formulation and Evaluation of Nitazoxanide Sustained-Release Matrix Tablets
... present study was to design and assess the twice-daily sustained-release matrix tablets of Nitazoxanide using different concentrations of hydrophilic ...for release during 12 h by using USP type- II ...
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Fabrication of Gelatin/Karaya gum blend microspheres for the controlled release of Distigmine bromide
... this study, semi IPN microspheres were fabricated from GE and KG by simple water-in-oil (w/o) emulsion cross- linking method using GA as a ...in vitro release study indicates the distigmine ...
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SIMVASTATIN LOADED NANO MIXED MICELLES: AN APPROACH TO TREAT HORMONE DEPENDENT CARCINOMAS
... In-vitro Release Study: In-vitro release profile of SMV from micelles and MMs was determined using dialysis method and was compared with the plain drug ...of release medium, PBS ...
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DESIGN AND CHARACTERIZATION OF PULSATILE TABLET IN CAPSULE DEVICE FOR HYPERTENSION THERAPY
... Prepared blend of ramipril was kept in hard gelatin capsule and dissolution studies were performed using a USP XXIII dissolution apparatus I (basket type) in 900 ml medium at 37º±0.5º C at a rotation speed of 50 rpm. In ...
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FORMULATION, ASSESSMENT AND COMPATIBILITY ANALYSIS OF DIFFERENT POLYMERS LOADED MICROSPHERES BY NON AQUEOUS SOLVENT EVAPORATION TECHNIQUE: IN VITRO IN VIVO STUDY OF GLIBENCLAMIDE AS A MODEL DRUG
... drug release pattern is not suitable similar to Diabetes mellitus, cardiovascular diseases and many more diseases, this present study has taken a challenge to formulate controlled release ...
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<p>Co-Delivery of Paclitaxel and Doxorubicin by pH-Responsive Prodrug Micelles for Cancer Therapy</p>
... In vitro drug release experiments and study on release mechanism showed that the drug release rate and accumulative release for PTX and DOX were dependent on the pH, showing the ...
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Preparation, characterization, and <em>in vitro</em> release study of albendazole-encapsulated nanosize liposomes
... present study was to formulate effective and controlled release albendazole liposomal ...this study, PEGylated and conventional liposomes containing albendazole were prepared and their ...
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“Development and Evaluation of Novel Site Specific Periodontal Film of Minocycline Hydrochloride for Periodontal Diseases” by Indira Raheja, Sushma Drabu, Kanchan Kohli, India.
... in vitro antibacterial activity. In vitro release from periodontal films was fit to different equations and kinetic models like zero order, first‐order equations and Hixson‐Crowell, Higuchi models ...
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FORMULATION AND EVALUATION OF BILAYER TABLETS OF SUSTAINED RELEASE NSAID’s AND IMMEDIATE RELEASE PROTON PUMP INHIBITOR
... in vitro drug release studies of Esomeprazole and Diclofenac sodium tablets were carried out using USP dissolution apparatus type- II (paddle type) at 50 rpm ...drug release was measured by UV ...
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DEVELOPMENT AND EVALUATION OF MICROSPONGE DRUG DELIVERY SYSTEM OF INDOMETHACIN
... in vitro dissolution study must be conducted in the dissolution medium which simulate the in-vivo conditions (actual physiological ...in vitro drug release studies for the prepared formulation ...
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Formulation and evaluation of atorvastatin calcium sustained release tablets
... the study was to develop the sustained release matrix tablets of various concentrations of natural and synthetic hydrophilic polymers on in-vitro release rate from the prepared Atorvastatin ...
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A WAY TO INCREASE EFFECTIVENESS OF PARACETAMOL DRUG THROUGH TRANSDERMAL PATCH
... as a plasticizer. To get better effect permeation enhancers such as Linseed oil and oleic acid was also incorporated and their optimum concentration was determined. Prepared formulations were evaluated for compatibility, ...
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DEVELOPMENT AND EVALUATION OF COMPRESSION COATED TIMED RELEASE TABLETS OF CANDESARTAN CILEXETIL FOR CHRONOTHERAPY OF HYPERTENSION
... The release profile with a lag time of 6 h and 100% release within next 1-2 h indicates the suitability of the formulation for the chronotherapy of hypertension where the tablet, when taken at bed time, ...
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FORMULATION AND INVITRO EVALUATION OF BUCCAL TABLETS OF PRAVASTATIN
... present study, an attempt was made to prepare Buccal tablets of Pravastatin HCL (HMG-CoA reductase inhibitors), in order to overcome bioavailability problems, to reduce dose dependent side effects Buccal tablets ...
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Biomedical applications of drug loaded protein-based polymer scaffolds and their in-vitro drug release profiles
... sustained release matrices (Li-Ya Huang, ...to study how it can be mixed with protein-based scaffolds to decline its transport complications in bio-systems and gastrointestinal side effects by adjusting its ...
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FORMULATION AND EVALUATION OF VALACYCLOVIR MUCOADHESIVE MICROSPHERE
... in vitro release behaviours. Infrared spectroscopic study confirmed the absence of any drug ‐ polymer ...in vitro release profile could be altered significantly by changing various ...
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Study of In Vitro Drug Release Profiles of Time-controlled Penta-layered Nanofiber Meshes
... this study is capable (i) for the development of more advanced and more efficient controlled-release drug delivery system and tissue engineering devices (ii) could provide multiphasic drug release ...
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