羟基磷灰石-角蛋白-聚乙烯醇复合基质中负载的废物衍生β磷酸三钙微珠在骨肉瘤治疗中的药物释放协同效应

IF 3.4 Q2 PHARMACOLOGY & PHARMACY Future Journal of Pharmaceutical Sciences Pub Date : 2024-08-28 DOI:10.1186/s43094-024-00681-7
Himanshi Diwan, Siddhartha Dan, Mahesh Kumar Sah
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引用次数: 0

摘要

背景用于临床相关骨肉瘤药物的持续给药系统(DDS)是一种前景广阔的治疗策略。在羟基磷灰石-角蛋白-聚乙烯醇复合基质支架(HAp-K-PVA)中载入盐酸多柔比星(DOX)和顺式二氨基二氯铂(CDDP)抗癌药物的β-磷酸三钙(β-TCP)微珠被开发为前景广阔的 DDS。开发 DDS 所用的 HAp、β-TCP 和 K 分别取自禽类蛋壳和人类毛发,并在应用前进行了适当的表征。结果将 DOX 和 CDDP 共同载入 DDS 后,在持续释放 30 天后观察到了协同效应,这与单独释放 DOX 和 CDDP 时的立即爆发形成了鲜明对比。此外,仅从微珠中释放药物时,HAp-K-PVA 复合基质支架的释放速度较慢。药物的可控释放、对测试病原体的抗菌效果以及成骨细胞样骨肉瘤(UTOS)细胞的存活率都表明了这种材料在原位治疗骨肉瘤方面的治疗潜力。在 24 小时内观察到的细胞存活率显示,HAp-K-PVA 复合基质支架的细胞存活率接近 90%,72 小时后所有支架组的细胞存活率均有所下降,这表明共负载药物的联合协同效应增强了细胞存活率。该研究为新型可持续生物材料治疗骨肉瘤奠定了良好的基础,其进一步发展有望提高患者的临床疗效,促进再生医学领域的进步。
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Synergistic effect of waste-derived β-tricalcium phosphate microbeads loaded in hydroxyapatite-keratin-polyvinyl alcohol composite matrix in drug release for osteosarcoma treatment

Background

Sustained drug delivery system (DDS) for clinically relevant osteosarcoma medications is a promising strategy for treatment. β-tricalcium phosphate (β-TCP) microbeads loaded with doxorubicin hydrochloride (DOX) and cis-diamminedichloroplatin (CDDP) anticancer drugs in a matrix of hydroxyapatite-keratin-polyvinyl alcohol composite matrix scaffolds (HAp-K-PVA) was developed as promising DDS. HAp, β-TCP, and K utilized for the development of DDS were resourced from avian eggshells and human hairs, respectively, and duly characterized before application.

Methods

The β-TCP/alginate microbeads were fabricated using droplet extrusion and ionotropic gelation, and integrated into secondary drug carrier HAp-K-PVA composite matrix, via freeze gelation. The physicochemical and thermal characterization of developed microbeads and matrix scaffolds was performed.

Results

When DOX and CDDP were co-loaded in DDS, a synergistic impact was observed after 30 days of continuous release, in contrast to the immediate outburst as seen with individual DOX and CDDP releases. Besides, the drug release from the microbeads only, the release with the HAp-K-PVA composite matrix scaffolds was observed slower. The controlled release, antibacterial effectiveness against the test pathogens and cell viability with osteoblast-like osteosarcoma (UTOS) cells indicated the therapeutic potential for the treatment of osteosarcoma in situ. The cell viability was observed for 24 h, which showed nearly 90% after 24 h for HAp-K-PVA composite matrix scaffolds, decreased for all the scaffold groups after 72 h, indicating the enhancement due to combined synergistic effect of the co-loaded drugs.

Conclusion

This study established a promising foundation for novel and sustainable biomaterials for osteosarcoma treatment. Further advancement holds the potential to enhance patient clinical outcomes and foster advancements in the field of regenerative medicine.

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来源期刊
自引率
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发文量
44
审稿时长
23 weeks
期刊介绍: Future Journal of Pharmaceutical Sciences (FJPS) is the official journal of the Future University in Egypt. It is a peer-reviewed, open access journal which publishes original research articles, review articles and case studies on all aspects of pharmaceutical sciences and technologies, pharmacy practice and related clinical aspects, and pharmacy education. The journal publishes articles covering developments in drug absorption and metabolism, pharmacokinetics and dynamics, drug delivery systems, drug targeting and nano-technology. It also covers development of new systems, methods and techniques in pharmacy education and practice. The scope of the journal also extends to cover advancements in toxicology, cell and molecular biology, biomedical research, clinical and pharmaceutical microbiology, pharmaceutical biotechnology, medicinal chemistry, phytochemistry and nutraceuticals.
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