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Initial design and physical characterization of a polymeric device for osmosis-driven delayed burst delivery of vaccines

机译:用于渗透驱动的疫苗延迟突发递送的聚合物装置的初步设计和物理表征

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摘要

Achieving the combination of delayed and immediate release of a vaccine from a delivery device without applying external triggers remains elusive in implementing single administration vaccination strategies. Here a means of vaccine delivery is presented, which exploits osmosis to trigger delayed burst release of an active compound. Poly(-caprolactone) capsules of 2 mm diameter were prepared by dip-coating, and their burst pressure and release characteristics were evaluated. Burst pressures (in bar) increased with wall thickness (t in mm) following Pburst = 131.t + 3.4 (R2 = 0.93). Upon immersion in PBS, glucose solution-filled capsules burst after 8.7 ± 2.9 days. Copolymers of hydrophobic  -caprolactone and hydrophilic polyethylene glycol were synthesized and their physico-chemical properties were assessed. With increasing hydrophilic content, the copolymer capsules showed increased water uptake rates and maximum weight increase, while the burst release was earlier: 5.6 ± 2.0 days and 1.9 ± 0.2 days for 5 and 10 wt% polyethylene glycol, respectively. The presented approach enables the reproducible preparation of capsules with high versatility in materials and properties, while these vaccine delivery vehicles can be prepared separately from, and independently of the active compound.
机译:在不使用外部触发装置的情况下,实现从递送装置延迟和立即释放疫苗的组合仍然难以实施单次接种疫苗策略。此处介绍了一种疫苗输送方法,该方法利用渗透作用来触发活性化合物的延迟爆炸释放。通过浸涂制备直径为2mm的聚(ε-己内酯)胶囊,并评价其破裂压力和释放特性。 Pburst = 131.t + 3.4(R2 = 0.93)后,爆裂压力(bar)随着壁厚(t以mm为单位)增加。浸入PBS后,葡萄糖溶液填充的胶囊在8.7±2.9天后破裂。合成了疏水性ε-己内酯和亲水性聚乙二醇的共聚物,并对其理化性质进行了评估。随着亲水含量的增加,共聚物胶囊显示出增加的吸水率和最大重量增加,而爆裂释放更早:对于5wt%和10wt%的聚乙二醇,分别为5.6±2.0天和1.9±0.2天。所提出的方法使得能够以可重复的方式制备具有高材料和特性通用性的胶囊,而这些疫苗递送载体可以与活性化合物分开并且独立于活性化合物来制备。

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