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壳聚糖对顺铂-羟基磷灰石-明胶复合微球载药量及释药的影响

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

作者信息

Wu Meng-Ying, Kao I-Fang, Yen Shiow-Kang

机构信息

Department of Materials Science and Engineering, National Chung Hsing University, Taichung 402, Taiwan.

Department of Orthopedics, Taichung Armed Forces General Hospital, Taichung 404, Taiwan.

出版信息

Polymers (Basel). 2025 May 27;17(11):1485. doi: 10.3390/polym17111485.


DOI:10.3390/polym17111485
PMID:40508728
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12158018/
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.

摘要

顺铂是一种广泛使用的化疗药物,但因其生物利用度低、全身清除快和副作用严重而受到限制。为了克服这些局限性,人们开发了羟基磷灰石-明胶复合微球,以提高药物包封率(DEE)并实现药物的持续释放。通过一次混合或采用连续包衣策略加入壳聚糖制备了各种制剂。通过调整负载程序,药物包封率从58%提高到了99%。复合微球有效地控制了药物的总释放持续时间,从一个月延长到了5个多月。此外,MTT试验表明,所有样品均能有效抑制细胞生长,实验2周后细胞活力降低至20%以下。这些发现表明,与一次性混合壳聚糖相比,连续壳聚糖包衣方法具有更好的药物包封和延长释放效果,显示出其作为癌症治疗持续给药系统的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/522d/12158018/4c96ecd8e90f/polymers-17-01485-g006a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/522d/12158018/1bdc56356b39/polymers-17-01485-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/522d/12158018/22b093f8d828/polymers-17-01485-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/522d/12158018/c4f2f185aab6/polymers-17-01485-g003a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/522d/12158018/18006b4b0abf/polymers-17-01485-g004a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/522d/12158018/c0128e2378c5/polymers-17-01485-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/522d/12158018/4c96ecd8e90f/polymers-17-01485-g006a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/522d/12158018/1bdc56356b39/polymers-17-01485-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/522d/12158018/22b093f8d828/polymers-17-01485-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/522d/12158018/c4f2f185aab6/polymers-17-01485-g003a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/522d/12158018/18006b4b0abf/polymers-17-01485-g004a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/522d/12158018/c0128e2378c5/polymers-17-01485-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/522d/12158018/4c96ecd8e90f/polymers-17-01485-g006a.jpg

相似文献

[1]
Effects of Chitosan on Drug Load and Release for Cisplatin-Hydroxyapatite-Gelatin Composite Microspheres.

Polymers (Basel). 2025-5-27

[2]
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[3]
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Polymers (Basel). 2022-10-12

[4]
[ study of bone morphogenetic protein 2 gelatin/chitosan hydrogel sustained-release system composite hydroxyapatite/zirconium dioxide foam ceramics and induced pluripotent stem cells derived mesenchymal stem cells].

Zhongguo Xiu Fu Chong Jian Wai Ke Za Zhi. 2019-2-15

[5]
Preparation and evaluation of the in vitro drug release properties and mucoadhesion of novel microspheres of hyaluronic acid and chitosan.

J Control Release. 2000-5-15

[6]
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Pharmaceutics. 2024-5-29

[7]
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Mater Sci Eng C Mater Biol Appl. 2019-3-11

[8]
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J Mater Chem B. 2014-3-7

[9]
Preparation and drug release property of tanshinone IIA loaded chitosan-montmorillonite microspheres.

Int J Biol Macromol. 2018-12-12

[10]
Chitosan-based mucoadhesive microspheres of clarithromycin as a delivery system for antibiotic to stomach.

Curr Drug Deliv. 2005-7

本文引用的文献

[1]
Nano-drug delivery system for the treatment of multidrug-resistant breast cancer: Current status and future perspectives.

Biomed Pharmacother. 2024-10

[2]
Reregulated mitochondrial dysfunction reverses cisplatin resistance microenvironment in colorectal cancer.

Smart Med. 2022-12-22

[3]
Recent advances in modified chitosan-based drug delivery systems for transmucosal applications: A comprehensive review.

Int J Biol Macromol. 2024-10

[4]
Porous Chitosan/Hydroxyapatite Composite Microspheres for Vancomycin Loading and Releasing.

Pharmaceutics. 2024-5-29

[5]
The Preparation and Characterization of Chitosan/Calcium Phosphate Composite Microspheres for Biomedical Applications.

Polymers (Basel). 2024-1-5

[6]
A green approach for preparation of chitosan/hydroxyapatite/graphitic carbon nitride hydrogel nanocomposite for improved 5-FU delivery.

Int J Biol Macromol. 2024-2

[7]
Gelatin-Functionalized Carbon Nanotubes Loaded with Cisplatin for Anti-Cancer Therapy.

Polymers (Basel). 2023-8-8

[8]
Effects of Adding Chitosan on Drug Entrapment Efficiency and Release Duration for Paclitaxel-Loaded Hydroxyapatite-Gelatin Composite Microspheres.

Pharmaceutics. 2023-7-26

[9]
High cancer selectivity and improving drug release from mesoporous silica nanoparticles in the presence of human serum albumin in cisplatin, carboplatin, oxaliplatin, and oxalipalladium treatment.

Eur J Pharm Sci. 2023-8-1

[10]
Anticancer and bone-enhanced nano-hydroxyapatite/gelatin/polylactic acid fibrous membrane with dual drug delivery and sequential release for osteosarcoma.

Int J Biol Macromol. 2023-6-15

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