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临床和临床前的人用疫苗热稳定性方法。

Clinical and Preclinical Methods of Heat-Stabilization of Human Vaccines.

机构信息

Division of Pharmacoengineering & Molecular Pharmaceutics, Eshelman School of Pharmacy, UNC, Chapel Hill, North Carolina 27599, United States.

Department of Biomedical Engineering, NC State/UNC, Chapel Hill, North Carolina 27695, United States.

出版信息

Mol Pharm. 2024 Mar 4;21(3):1015-1026. doi: 10.1021/acs.molpharmaceut.3c00844. Epub 2024 Jan 30.

Abstract

Vaccines have historically faced challenges regarding stability, especially in regions lacking a robust cold chain infrastructure. This review delves into established and emergent techniques to improve the thermostability of vaccines. We discuss the widely practiced lyophilization method, effectively transforming liquid vaccine formulations into a solid powdered state, enhancing storage and transportation ability. However, potential protein denaturation during lyophilization necessitates alternative stabilization methods. Cryoprotectants, namely, starch and sugar molecules, have shown promise in protecting vaccine antigens and adjuvants from denaturation and augmenting the stability of biologics during freeze-drying. Biomineralization, a less studied yet innovative approach, utilizes inorganic or organic-inorganic hybrids to encapsulate biological components of vaccines with a particular emphasis on metal-organic coordination polymers. Encapsulation in organic matrices to form particles or microneedles have also been studied in the context of vaccine thermostability, showing some ability to store outside the cold-chain. Unfortunately, few of these techniques have advanced to clinical trials that evaluate differences in storage conditions. Nonetheless, early trials suggest that alternative storage techniques are viable and emphasize the need for more comprehensive studies. This review underscores the pressing need for heat-stable vaccines, especially in light of the increasing global distribution challenges. Combining traditional methods with novel approaches holds promise for the future adaptability of vaccine distribution and use.

摘要

疫苗在稳定性方面一直面临挑战,特别是在缺乏健全冷链基础设施的地区。本综述深入探讨了已建立和新兴的技术,以提高疫苗的热稳定性。我们讨论了广泛应用的冷冻干燥法,它将液态疫苗制剂有效地转化为固态粉末状态,提高了储存和运输能力。然而,冷冻干燥过程中潜在的蛋白质变性需要替代的稳定化方法。冷冻保护剂,即淀粉和糖分子,已显示出保护疫苗抗原和佐剂免受变性的潜力,并增强了生物制品在冷冻干燥过程中的稳定性。生物矿化,一种研究较少但创新的方法,利用无机或有机-无机杂化物来封装疫苗的生物成分,特别强调金属-有机配位聚合物。在疫苗热稳定性方面,也研究了在有机基质中形成颗粒或微针的封装,表明它们具有在冷链外储存的能力。然而,这些技术中很少有进展到临床试验,以评估存储条件的差异。尽管如此,早期试验表明替代存储技术是可行的,并强调需要进行更全面的研究。本综述强调了对热稳定疫苗的迫切需求,特别是考虑到日益增加的全球分发挑战。将传统方法与新方法相结合,为疫苗分发和使用的未来适应性提供了希望。

相似文献

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Clinical and Preclinical Methods of Heat-Stabilization of Human Vaccines.临床和临床前的人用疫苗热稳定性方法。
Mol Pharm. 2024 Mar 4;21(3):1015-1026. doi: 10.1021/acs.molpharmaceut.3c00844. Epub 2024 Jan 30.
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Micro and nanotechnologies: The little formulations that could.微米和纳米技术:小制剂的大作为。
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