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Considerations in the sterile manufacture of polymeric microneedle arrays

机译:无菌制造聚合物微针阵列的注意事项

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We describe, for the first time, considerations in the sterile manufacture of polymeric microneedle arrays. Microneedles (MN) made from dissolving polymeric matrices and loaded with the model drugs ovalbumin (OVA) and ibuprofen sodium and hydrogel-forming MN composed of "super-swelling" polymers and their corresponding lyophilised wafer drug reservoirs loaded with OVA and ibuprofen sodium were prepared aseptically or sterilised using commonly employed sterilisation techniques. Moist and dry heat sterilisation, understandably, damaged all devices, leaving aseptic production and gamma sterilisation as the only viable options. No measureable bioburden was detected in any of the prepared devices, and endotoxin levels were always below the US Food & Drug Administration limits (20 endotoxin units/device). Hydrogel-forming MN were unaffected by gamma irradiation (25 kGy) in terms of their physical properties or capabilities in delivering OVA and ibuprofen sodium actoss excised neonatal porcine skin in vitro. However, OVA content in dissolving MN (down from approximately 101.1 °/o recovery to approximately 58.3 % recovery) and lyophilised wafer-type drug reservoirs (down from approximately 99.7 % recovery to approximately 60.1 % recovery) was significantly reduced by gamma irradiation, while the skin permeation profile of ibuprofen sodium from gamma-irradiated dissolving MN was markedly different from their non-irradiated counterparts. It is clear that MN poses a very low risk to human health when used appropriately, as evidenced here by low endotoxin levels and absence of microbial contamination. However, if guarantees of absolute sterility of MN products are ultimately required by regulatory authorities, it will be necessary to investigate the effect of lower gamma doses on dissolving MN loaded with active pharmaceutical ingredients and lyophilised wafers loaded with biomolecules in order to avoid the expense and inconvenience of aseptic processing.
机译:我们首次描述了无菌制造聚合物微针阵列的考虑因素。制备了由溶解聚合物基质制成的,装有模型药物卵清蛋白(OVA)和布洛芬钠的微针(MN),以及由“超溶胀”聚合物组成的水凝胶形成的MN及其相应的装有OVA和布洛芬钠的冻干威化片药库。无菌或使用常用的灭菌技术进行灭菌。可以理解,潮湿和干燥的热灭菌会损坏所有设备,而无菌生产和伽马灭菌是唯一可行的选择。在任何准备好的设备中均未检测到可测量的生物负荷,并且内毒素水平始终低于美国食品药品监督管理局的限值(每台设备20个内毒素单位)。形成水凝胶的MN的物理特性或在体外输送OVA和布洛芬钠肌酸的新生猪皮肤的递送能力不受γ射线(25 kGy)的影响。然而,γ辐照显着降低了溶解性MN中的OVA含量(从约101.1°/ o的回收率降低至约58.3%的回收率)和冻干威化饼型药物库(从约99.7%的回收率降低至约60.1%的回收率),同时γ射线辐照的溶解性MN中布洛芬钠的皮肤渗透曲线与未辐照的MN明显不同。显然,如适当使用,MN对人类健康的危害非常低,如内毒素水平低和无微生物污染所证明。但是,如果监管机构最终需要保证MN产品的绝对无菌,则有必要研究较低的伽玛剂量对溶解有活性药物成分的MN和装有生物分子的冻干薄饼的溶解效果,以避免费用和无菌处理的不便。

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