Purpose: The objective of the present study was to prepare and evaluate microcapsules for the controlled release of lamivudine using various cellulose polymers Methods: The microcapsules were prepared by the solvent evaporation method. The prepared microcapsules were characterized for the percent drug content, entrapment efficiency, FTIR, DSC, scanning electron microscopy (SEM) and in vitro dissolution studies. Accelerated stability studies were also carried out. Results: The microcapsules were spherical and free flowing. The entrapment efficiency was 76-86%. The release of drug from the microcapsules extended up to 8 to 12 hours. FTIR and DSC thermograms showed the stable character of lamivudine in the microcapsules. SEM revealed that t...
Nimesulide was formulated as sustained release microcapsules using biodegradable polymer Poly(D,L-l...
For the development of any formulation, techniques such as thermal and isothermal stress testing wer...
The objective of this study was to formulate and evaluate the drug-polymer interaction of mefenamic ...
Purpose: The objective of the present study was to prepare and evaluate microcapsules for the contro...
The present study was undertaken to develop controlled release osmotic pump tablets of lamivudine a ...
PURPOSE: The present work reports the study of different proportion of Lamivudine: Methocel K15M for...
Objective: The objective of the present study was to investigate the possibility of obtaining a cont...
Objective: The objective of this study was to design and evaluate controlled release mucoadhesive mi...
Aim and objective: The aim of the study was to formulate and evaluate Transferosomal gel of lamivudi...
The aim of present study was to formulate & evaluate the mucoadhesive sustained release formulat...
ABSTRACT: Nanoparticles represent a promising drug delivery system of controlled and targeted drug r...
controlled release; chitosan; hydroxypropyl methylcellulose. The objective of present study was to d...
Purpose: The aim of this study was to formulate and evaluate microencapsulated controlled release pr...
The aim of present study was to formulate & evaluate the mucoadhesive sustained release formulat...
Lamivudine nanoparticles were prepared by Ionotropic pregelation method by optimizing the parameters...
Nimesulide was formulated as sustained release microcapsules using biodegradable polymer Poly(D,L-l...
For the development of any formulation, techniques such as thermal and isothermal stress testing wer...
The objective of this study was to formulate and evaluate the drug-polymer interaction of mefenamic ...
Purpose: The objective of the present study was to prepare and evaluate microcapsules for the contro...
The present study was undertaken to develop controlled release osmotic pump tablets of lamivudine a ...
PURPOSE: The present work reports the study of different proportion of Lamivudine: Methocel K15M for...
Objective: The objective of the present study was to investigate the possibility of obtaining a cont...
Objective: The objective of this study was to design and evaluate controlled release mucoadhesive mi...
Aim and objective: The aim of the study was to formulate and evaluate Transferosomal gel of lamivudi...
The aim of present study was to formulate & evaluate the mucoadhesive sustained release formulat...
ABSTRACT: Nanoparticles represent a promising drug delivery system of controlled and targeted drug r...
controlled release; chitosan; hydroxypropyl methylcellulose. The objective of present study was to d...
Purpose: The aim of this study was to formulate and evaluate microencapsulated controlled release pr...
The aim of present study was to formulate & evaluate the mucoadhesive sustained release formulat...
Lamivudine nanoparticles were prepared by Ionotropic pregelation method by optimizing the parameters...
Nimesulide was formulated as sustained release microcapsules using biodegradable polymer Poly(D,L-l...
For the development of any formulation, techniques such as thermal and isothermal stress testing wer...
The objective of this study was to formulate and evaluate the drug-polymer interaction of mefenamic ...