Abstract
Aim: The aim of the present study is to prepare Diltiazem HCl loaded Bovine Serum Albumin nanoparticles by Desolvation technique using Isopropanol as desolvating agent. Here in this study, attempts have been made to prepare Diltiazem loaded BSA nanoparticles by Desolvation technique.
Methodology: Two methods were followed in the process of adding desolvating agent to aqueous solution of BSA; continuous addition method and intermittent addition method. In continuous addition method, the desolvating agent was added at the rate of 1ml per minute, whereas, in intermittent addition method, the desolvating agent was added at the rate of 1ml per every five minutes. The effects of continuous and intermittent addition methods on nanoparticles size, stability, loading capacity, encapsulation efficiency and in vitro drug release were studied. The particle size and stability of the formulations were determined by Horiba SZ 100 series particle size analyzer. Encapsulation efficiency and loading capacity were determined by ELTEK NP 400 Ultracentrifuge.
Results: The particle size was 267.3nm and 257.8nm, and encapsulation efficiency was found to be 90.3% and 95% Comparative study was performed to determine the best method for the preparation of Diltiazem nanoparticles.
Conclusion: On comparison, intermittent addition method was considered to be the best method for the preparation of Diltiazem HCl loaded BSA nanoparticles because of the smaller particle size and greater stability and encapsulation efficiency. The drug release was sustained till 12hrs for nanoparticles prepared by intermittent addition method.
Keywords: Desolvation BSA, diltiazem HCl, nanoparticles, particle size, polymer matrix, stability.
Graphical Abstract
Pharmaceutical Nanotechnology
Title:Preparation and Characterization of Diltiazem HCL Loaded Bovine Serum Albumin Nanoparticles by Desolvation Technique
Volume: 4 Issue: 4
Author(s): Krishna A. Sailaja and Vutpala Sreelola
Affiliation:
Keywords: Desolvation BSA, diltiazem HCl, nanoparticles, particle size, polymer matrix, stability.
Abstract: Aim: The aim of the present study is to prepare Diltiazem HCl loaded Bovine Serum Albumin nanoparticles by Desolvation technique using Isopropanol as desolvating agent. Here in this study, attempts have been made to prepare Diltiazem loaded BSA nanoparticles by Desolvation technique.
Methodology: Two methods were followed in the process of adding desolvating agent to aqueous solution of BSA; continuous addition method and intermittent addition method. In continuous addition method, the desolvating agent was added at the rate of 1ml per minute, whereas, in intermittent addition method, the desolvating agent was added at the rate of 1ml per every five minutes. The effects of continuous and intermittent addition methods on nanoparticles size, stability, loading capacity, encapsulation efficiency and in vitro drug release were studied. The particle size and stability of the formulations were determined by Horiba SZ 100 series particle size analyzer. Encapsulation efficiency and loading capacity were determined by ELTEK NP 400 Ultracentrifuge.
Results: The particle size was 267.3nm and 257.8nm, and encapsulation efficiency was found to be 90.3% and 95% Comparative study was performed to determine the best method for the preparation of Diltiazem nanoparticles.
Conclusion: On comparison, intermittent addition method was considered to be the best method for the preparation of Diltiazem HCl loaded BSA nanoparticles because of the smaller particle size and greater stability and encapsulation efficiency. The drug release was sustained till 12hrs for nanoparticles prepared by intermittent addition method.
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Sailaja A. Krishna and Sreelola Vutpala, Preparation and Characterization of Diltiazem HCL Loaded Bovine Serum Albumin Nanoparticles by Desolvation Technique, Pharmaceutical Nanotechnology 2016; 4 (4) . https://dx.doi.org/10.2174/2211738504666160519144841
DOI https://dx.doi.org/10.2174/2211738504666160519144841 |
Print ISSN 2211-7385 |
Publisher Name Bentham Science Publisher |
Online ISSN 2211-7393 |

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