Effects of Chitosan on Drug Load and Release for Cisplatin–Hydroxyapatite–Gelatin Composite Microspheres

Cisplatin, a widely used chemotherapeutic agent, is limited by its poor bioavailability, rapid systemic clearance, and severe side effects. To overcome these limitations, hydroxyapatite-gelatin composite microspheres were developed to improve drug entrapment efficiency (DEE) and provide sustained drug release. Various formulations were prepared by incorporating chitosan either by mixing once or through a sequential coating strategy. By adjusting the loading procedure, the DEE increased from 58% to 99%. The composite microsphere effectively controlled the total drug release duration, extending it from one month to over 5 months. Moreover, the MTT assay demonstrated that all samples effectively inhibited cell growth, with cell viability reduced to less than 20% after 2 weeks of experimentation. These findings demonstrate that the sequential chitosan coating method offers superior drug entrapment and prolonged release compared to mixing chitosan once, exhibiting its potential as a sustained drug delivery system for cancer treatment.

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Publication Details

Journal
Polymers
Published
2025-05-27
DOI
https://doi.org/10.3390/polym17111485
Citations
2
Primary Topic
Advanced Drug Delivery Systems
Type
article
Field-Weighted Citation Impact
1.58

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article

Effects of Chitosan on Drug Load and Release for Cisplatin–Hydroxyapatite–Gelatin Composite Microspheres

Shiow‐Kang Yen, Mengying Wu, I-Fang Kao
2 citations
Polymers
Advanced Drug Delivery Systems
1.58
article

Effects of Chitosan on Drug Load and Release for Cisplatin–Hydroxyapatite–Gelatin Composite Microspheres

Shiow‐Kang Yen, Mengying Wu, I-Fang Kao
article en
2 citations

Abstract

Cisplatin, a widely used chemotherapeutic agent, is limited by its poor bioavailability, rapid systemic clearance, and severe side effects. To overcome these limitations, hydroxyapatite-gelatin composite microspheres were developed to improve drug entrapment efficiency (DEE) and provide sustained drug release. Various formulations were prepared by incorporating chitosan either by mixing once or through a sequential coating strategy. By adjusting the loading procedure, the DEE increased from 58% to 99%. The composite microsphere effectively controlled the total drug release duration, extending it from one month to over 5 months. Moreover, the MTT assay demonstrated that all samples effectively inhibited cell growth, with cell viability reduced to less than 20% after 2 weeks of experimentation. These findings demonstrate that the sequential chitosan coating method offers superior drug entrapment and prolonged release compared to mixing chitosan once, exhibiting its potential as a sustained drug delivery system for cancer treatment.

PolymersVol. 17(11)
National Chung Hsing University (TW), Nanhua University (TW), Taichung Armed Forces General Hospital (TW), Central Taiwan University of Science and Technology (TW)
National Science and Technology Council
Openalex Percentile: Top 17%
Advanced Drug Delivery Systems
1.58
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