Acyclovir entrapped niosomes were prepared by hand shaking and ether injection process with different ratios of (1:1, 1;2 and 1:3) cholesterol (CHOL) and Span-80 (Non-ionic surfactant).The niosomes prepared were in the size range of 0.5-5 microns in the case of hand shaking process and 0.5-2.5 microns in the case of Ether injection process. The order of encapsulation efficiency increases when span-80 concentration was increased. In-vitro release study on acyclovir niosomes indicates 76.64 % release for formulation prepared with CHOL: Span-80 (1:1) and it takes an extended period of 1 day and 16 h for release
BACKGROUND: Development of new drug carriers would be an interesting approach if it allowed increas...
Received on:25-12-2008; Accepted on:26-02-2009 The poor bioavailability and therapeutic response exh...
controlled release; chitosan; hydroxypropyl methylcellulose. The objective of present study was to d...
A review on proniosomal drug delivery system for targeted drug action Proniosomes are dry formulatio...
Objective: The objective of this study was to formulate and evaluate liposomes loaded with acyclovir...
Acyclovir (ACV), analog of 2′-deoxyguanosine, is known for its antiviral activity against Herpes ...
Niosomes are efficient carriers for controlled drug delivery, to entrap hydrophilic drugs in the lar...
Objective: The objective of this study was to formulate and evaluate liposomes loaded with acyclovir...
Objective: The objective of the study was to perform a screening, optimization of valacyclovir nioso...
Objective: The objective of the study was to perform a screening, optimization of valacyclovir nioso...
The objective of the present investigation was to formulate and evaluate hydrodynamically balanced f...
In the present study, 33 factorial design was used to investigate the combined influence of three in...
BACKGROUND: Development of new drug carriers would be an interesting approach if it allowed increas...
Background: Development of new drug carriers would be an interesting approach if it allowed increase...
BACKGROUND: Development of new drug carriers would be an interesting approach if it allowed increas...
BACKGROUND: Development of new drug carriers would be an interesting approach if it allowed increas...
Received on:25-12-2008; Accepted on:26-02-2009 The poor bioavailability and therapeutic response exh...
controlled release; chitosan; hydroxypropyl methylcellulose. The objective of present study was to d...
A review on proniosomal drug delivery system for targeted drug action Proniosomes are dry formulatio...
Objective: The objective of this study was to formulate and evaluate liposomes loaded with acyclovir...
Acyclovir (ACV), analog of 2′-deoxyguanosine, is known for its antiviral activity against Herpes ...
Niosomes are efficient carriers for controlled drug delivery, to entrap hydrophilic drugs in the lar...
Objective: The objective of this study was to formulate and evaluate liposomes loaded with acyclovir...
Objective: The objective of the study was to perform a screening, optimization of valacyclovir nioso...
Objective: The objective of the study was to perform a screening, optimization of valacyclovir nioso...
The objective of the present investigation was to formulate and evaluate hydrodynamically balanced f...
In the present study, 33 factorial design was used to investigate the combined influence of three in...
BACKGROUND: Development of new drug carriers would be an interesting approach if it allowed increas...
Background: Development of new drug carriers would be an interesting approach if it allowed increase...
BACKGROUND: Development of new drug carriers would be an interesting approach if it allowed increas...
BACKGROUND: Development of new drug carriers would be an interesting approach if it allowed increas...
Received on:25-12-2008; Accepted on:26-02-2009 The poor bioavailability and therapeutic response exh...
controlled release; chitosan; hydroxypropyl methylcellulose. The objective of present study was to d...