CALIBRATING HYDROGELS FOR DELIVERY OF BIOLOGICS

K. Pathak
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引用次数: 1

Abstract

In the past decade, depot systems for tissue engineering, cell therapy, biomedical research, and therapeutic proteins, have been extensively investigated. Hydrogels offer an interesting platform for sustained delivery of biologicals as these can be readily formulated with limited impact on their integrity and stability. Their high-water content and porous structures make them especially suitable for loading with therapeutic proteins However, relatively rapid release of the hydrophilic compounds (period of hours to days) and limited drug loading capacity (<10%) present major challenges. Cleavable cross-linker or hydrogels that respond to an external trigger such as ultrasound have been suggested as suitable alternatives. However, scale-up and cost-effective manufacturing using safe and established excipients remains a challenge and hydrogels for biologicals are at present scarcely developed beyond the clinical evaluation phases. While some commercial products are available the future of hydrogels for biologicals depends on the medical needs, the general benefit/risk balance, and overall costs.
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校准用于输送生物制剂的水凝胶
在过去的十年中,组织工程、细胞治疗、生物医学研究和治疗性蛋白质的仓库系统得到了广泛的研究。水凝胶为生物制剂的持续递送提供了一个有趣的平台,因为这些生物制剂可以很容易地配制,对其完整性和稳定性的影响有限。它们的高含水量和多孔结构使它们特别适合装载治疗性蛋白质。然而,亲水性化合物的相对快速释放(数小时至数天)和有限的药物装载能力(<10%)是主要的挑战。可切割的交联剂或水凝胶响应外部触发,如超声已被建议为合适的替代品。然而,使用安全和成熟的赋形剂进行大规模和具有成本效益的生产仍然是一个挑战,生物制剂的水凝胶目前几乎没有开发出临床评估阶段。虽然有一些商业产品,但水凝胶用于生物制品的未来取决于医疗需求、总体收益/风险平衡和总体成本。
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