Jeong Hye-Seon, Kim Eunseo, Park Jong Pil, Lee Sei-Jung, Lee Hyomin, Choi Chang-Hyung
School of Chemical Engineering, Yeungnam University, 280 Daehak-ro, Gyeongsan, Gyeongbuk 38541, Republic of Korea; Division of Cosmetic Science and Technology, Daegu Haany University, 1 Haanydaero, Gyeongsan, Gyeongbuk 38610, Republic of Korea.
Department of Chemical Engineering, Pohang University of Science and Technology (POSTECH), 77 Cheongam-Ro, Nam-Gu, Pohang, Gyeongbuk 37673, Republic of Korea.
J Control Release. 2023 Apr;356:337-346. doi: 10.1016/j.jconrel.2023.02.045. Epub 2023 Mar 9.
Here, we report PNIPAm-co-PEGDA hydrogel shelled microcapsules with a thin oil layer to achieve tunable thermo-responsive release of the encapsulated small hydrophilic actives. We use a microfluidic device integrated with a temperature-controlled chamber for consistent and reliable production of the microcapsules by utilizing triple emulsion drops (W/O/W/O) with a thin oil layer as capsule templates. The interstitial oil layer between the aqueous core and the PNIPAm-co-PEGDA shell provides a diffusion barrier for the encapsulated active until the temperature reaches a critical point above which the destabilization of interstitial oil layer occurs. We find that the destabilization of the oil layer with temperature increase is caused by outward expansion of the aqueous core due to volume increase and the radial inward compression from the deswelling of the thermo-responsive hydrogel shell. The copolymerization of NIPAm with PEGDA increases the biocompatibility of the resulting microcapsule while offering the ability to alter the compressive modulus in broad ranges by simply varying crosslinker concentrations thereby to precisely tune the onset release temperature. Based on this concept, we further demonstrate that the release temperature can be enhanced up to 62 °C by adjusting the shell thickness even without varying the chemical composition of the hydrogel shell. Moreover, we incorporate gold nanorods within the hydrogel shell to spatiotemporally regulate the active release from the microcapsules by illuminating with non-invasive near infrared (NIR) light.
在此,我们报道了具有薄油层的聚N-异丙基丙烯酰胺-共-聚乙二醇二丙烯酸酯(PNIPAm-co-PEGDA)水凝胶包壳微胶囊,以实现对包封的亲水性小分子活性物质的可调热响应释放。我们使用集成了温度控制腔室的微流控装置,通过利用具有薄油层的三重乳液滴(W/O/W/O)作为胶囊模板,来一致且可靠地生产微胶囊。水核与PNIPAm-co-PEGDA壳之间的间隙油层为包封的活性物质提供了扩散屏障,直到温度达到临界点,此时间隙油层会发生失稳。我们发现,随着温度升高油层的失稳是由于水核因体积增加而向外膨胀以及热响应水凝胶壳的溶胀导致的径向向内压缩所引起的。NIPAm与PEGDA的共聚增加了所得微胶囊的生物相容性,同时通过简单改变交联剂浓度能够在很宽的范围内改变压缩模量,从而精确调节起始释放温度。基于这一概念,我们进一步证明,即使不改变水凝胶壳的化学成分,通过调节壳厚度也可将释放温度提高到62°C。此外,我们在水凝胶壳内掺入金纳米棒,通过非侵入性近红外(NIR)光照射来时空调节微胶囊中活性物质的释放。