Ashkenazi Shaked, Matsanov Pnina, Nassar-Marjiya Eid, Farah Shady, Weitz Iris S
Department of Biotechnology Engineering, Braude College of Engineering Karmiel, Karmiel 2161002, Israel.
The Laboratory for Advanced Functional/Medicinal Polymers & Smart Drug Delivery Technologies, The Wolfson Faculty of Chemical Engineering, Technion - Israel Institute of Technology, Haifa 3200003, Israel.
ACS Omega. 2024 Mar 5;9(11):13382-13390. doi: 10.1021/acsomega.3c10447. eCollection 2024 Mar 19.
A nanocapsule shell of poly(ethylene glycol)--poly(d,l-lactic acid) (PEG--PLA) mixed with anionic Eudragit S100 (90/10% w/w) was previously used to entrap and define the self-assembly of indigo carmine (IC) within the hydrophilic cavity core. In the present work, binary blends were prepared by solution mixing at different PEG--PLA/Eudragit S100 ratios (namely, 100/0, 90/10, 75/25, and 50/50% w/w) to elucidate the role of the capsule shell in tuning the encapsulation of the anionic dye (i.e., IC). The results showed that the higher content of Eudragit S100 in the blend decreases the miscibility of the two polymers due to weak intermolecular interactions between PEG--PLA and Eudragit S100. Moreover, with an increase in the amount of Eudragit S100, a higher thermal stability was observed related to the mobility restriction of PEG--PLA chains imposed by Eudragit S100. Formulations containing 10 and 25% Eudragit S100 exhibited an optimal interplay of properties between the negative surface charge and the miscibility of the polymer blend. Therefore, the anionic character of the encapsulating agent provides sufficient accumulation of IC molecules in the nanocapsule core, leading to dye aggregates following the self-assembly. At the same time, the blending of the two polymers tunes the IC release properties in the initial stage, achieving slow and controlled release. These findings give important insights into the rational design of polymeric nanosystems containing organic dyes for biomedical applications.
先前使用聚(乙二醇)-聚(d,l-乳酸)(PEG-PLA)与阴离子型丙烯酸树脂S100(90/10% w/w)混合的纳米胶囊壳来包裹靛蓝胭脂红(IC)并确定其在亲水腔核内的自组装情况。在本工作中,通过溶液混合以不同的PEG-PLA/丙烯酸树脂S100比例(即100/0、90/10、75/25和50/50% w/w)制备二元共混物,以阐明胶囊壳在调节阴离子染料(即IC)包封方面的作用。结果表明,共混物中丙烯酸树脂S100含量越高,由于PEG-PLA与丙烯酸树脂S100之间的分子间相互作用较弱,两种聚合物的混溶性降低。此外,随着丙烯酸树脂S100用量的增加,观察到更高的热稳定性,这与丙烯酸树脂S100对PEG-PLA链的迁移限制有关。含有10%和25%丙烯酸树脂S100的制剂在负表面电荷和聚合物共混物的混溶性之间表现出最佳的性能相互作用。因此,包封剂的阴离子特性使IC分子在纳米胶囊核心中充分积累,导致自组装后形成染料聚集体。同时,两种聚合物的共混在初始阶段调节了IC的释放特性,实现了缓慢且可控的释放。这些发现为用于生物医学应用的含有机染料的聚合物纳米系统的合理设计提供了重要见解。