2012•Science & Technology in Chemical IndustryRequires access

Preparation of drug loaded gelatin microspheres and release behaviour in vitro

Zhongjin Li

Open publisher page 0 citations

Abstract

In this study,the aspirin loaded gelatin microspheres were prepared using aspirin as the drug model molecules.The SEM result showed that the surface structure of microspheres was more compact after drug loading.The drug loading property of microspheres was investigated,which showed that the drug loading property(drug loading capacity was 7.3% and encapsulation efficiency was 57.5%) was optimum as the aspirin dosage was 16 mg.The drug release properties of the gelatin microspheres in artificial body fluid were explored,good sustained release properties of gelatin microspheres were observed.And the release efficiency is much higher in the artificial gastric juice due to the larger presence of acid and pepsin,drug release rates in artificial gastric juice and artificial intestinal fluid were 28% and 40% respectively.The first order dynamic model could describe the release process in vitro perfectly.

About this research paper

What this paper is about

In this study,the aspirin loaded gelatin microspheres were prepared using aspirin as the drug model molecules.The SEM result showed that the surface structure of microspheres was more compact after drug loading.The drug loading property of microspheres was investigated,which showed that the drug loading property(drug loading capacity was 7.3% and encapsulation efficiency was 57.5%) was optimum as the aspirin dosage was 16 mg.The drug release properties of the gelatin microspheres in artificial body fluid were explored,good sustained release properties of gelatin microspheres were observed.And the release efficiency is much higher in the artificial gastric juice due to the larger presence of acid and pepsin,drug release rates in artificial gastric juice and artificial intestinal fluid were 28% and 40% respectively.The first order dynamic model could describe the release process in vitro perfectly.

Why it matters

A significance statement is not available in the OpenAlex record.

Key contribution

A contribution statement is not available in the OpenAlex record.

Method / approach

Method details are not available in the OpenAlex metadata.

Main findings

Findings are not separately available in the OpenAlex metadata.

Limitations

Limitations are not available in the OpenAlex metadata.

Applications

Application details are not available in the OpenAlex metadata.

Available abstract

In this study,the aspirin loaded gelatin microspheres were prepared using aspirin as the drug model molecules.The SEM result showed that the surface structure of microspheres was more compact after drug loading.The drug loading property of microspheres was investigated,which showed that the drug loading property(drug loading capacity was 7.3% and encapsulation efficiency was 57.5%) was optimum as the aspirin dosage was 16 mg.The drug release properties of the gelatin microspheres in artificial body fluid were explored,good sustained release properties of gelatin microspheres were observed.And the release efficiency is much higher in the artificial gastric juice due to the larger presence of acid and pepsin,drug release rates in artificial gastric juice and artificial intestinal fluid were 28% and 40% respectively.The first order dynamic model could describe the release process in vitro perfectly.

Key concepts: Gelatin, Drug, Microsphere, Chemistry, Chromatography, Dosage form, Gastric fluid, Aspirin

Related papers

Back to paper searchBrowse research topicsOriginal source
Preparation of drug loaded gelatin microspheres and release behaviour in vitro — Research Paper | ScholarLens