School of Engineering and Material Science, Queen Mary University of London, Mile End, London, E1 4NS, UK.
Institute of Dentistry, Bart's and the London, School of Medicine and Dentistry, Queen Mary University of London, London, E1 2AT, UK.
Soft Matter. 2020 Mar 4;16(9):2266-2275. doi: 10.1039/c9sm01856e.
The encapsulation of small hydrophilic molecules and response to specific biological triggers in a controlled manner have become two of the significant challenges in biomedical research, in particular in the field of localized drug delivery and biosensing. This work reports the fabrication of free-standing microchamber array films made of biodegradable polymers for the encapsulation and enzymatically triggered release of small hydrophilic molecules. Polycaprolactone (PCL) microchamber arrays were demonstrated to fully biodegrade within 5 hours of exposure to lipase from Pseudomonas cepacia (lipase PS) at a concentration of 0.5 mg ml-1, with lower concentrations producing correspondingly longer degradation times. The gradual process of deterioration was real-time monitored utilising laser Fraunhofer diffraction patterns. Additionally, a small hydrophilic molecule, 5(6)-carboxyfluorescein (CF), was loaded into the PCL microchamber arrays in a dry state; however, the substantial permeability of the PCL film led to leakage of the dye molecules. Consequently, polylactic acid (PLA) was blended with PCL to reduce its permeability, enabling blended PCL-PLA (1 : 2 ratio correspondingly) microchamber arrays to trap the small hydrophilic molecule CF. PCL-PLA (1 : 2) microchamber arrays hold potential for controlled release under the catalysis of lipase within 26 hours. Additionally, it is calculated that approximately 11 pg of CF dye crystals was loaded into individual microchambers of 10 μm size, indicating that the microchamber array films could yield a highly efficient encapsulation.
以可控的方式将小分子亲水性分子包封并对特定的生物触发因素做出响应已成为生物医学研究,特别是局部药物输送和生物传感领域的两个重大挑战。这项工作报道了由可生物降解聚合物制成的独立微室阵列膜的制造,用于包封和酶触发释放小分子亲水性分子。聚己内酯(PCL)微室阵列在浓度为 0.5mgml-1 的假单胞菌脂肪酶(脂肪酶 PS)暴露 5 小时内完全生物降解,较低的浓度会产生相应更长的降解时间。利用激光夫琅和费衍射模式实时监测逐渐恶化的过程。此外,将小分子亲水性分子 5(6)-羧基荧光素(CF)以干燥状态装入 PCL 微室阵列中;然而,PCL 膜的高渗透性导致染料分子泄漏。因此,将聚乳酸(PLA)与 PCL 混合以降低其渗透性,使混合的 PCL-PLA(相应的 1:2 比例)微室阵列能够捕获小分子亲水性分子 CF。PCL-PLA(1:2)微室阵列在脂肪酶的催化下具有在 26 小时内进行控制释放的潜力。此外,计算得出大约 11pg 的 CF 染料晶体被装入 10μm 大小的单个微室中,表明微室阵列膜可以实现高效封装。