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用于口服递送疏水性化合物的无表面活性剂电喷雾海藻酸盐珠粒

Surfactant-Free Electrosprayed Alginate Beads for Oral Delivery of Hydrophobic Compounds.

作者信息

Jeong Hye-Seon, Kim Hyo-Jin, Kang Sung-Min, Choi Chang-Hyung

机构信息

School of Chemical Engineering, Yeungnam University, 280, Daehak-ro, Gyeongsan 38541, Republic of Korea.

Department of Green Chemical Engineering, Sangmyung University, Cheonan 31066, Republic of Korea.

出版信息

Polymers (Basel). 2025 Jul 30;17(15):2098. doi: 10.3390/polym17152098.

Abstract

Oral delivery of hydrophobic compounds remains challenging due to their poor aqueous solubility and the potential toxicity associated with conventional surfactant-based emulsions. To address these issues, we present a surfactant-free encapsulation strategy using electrosprayed alginate hydrogel beads for the stable and controlled delivery of hydrophobic oils. Hydrophobic compounds were dispersed in high-viscosity alginate solutions without surfactants via ultrasonication, forming kinetically stable oil-in-water dispersions. These mixtures were electrosprayed into calcium chloride baths, yielding monodisperse hydrogel beads. Higher alginate concentrations improved droplet sphericity and suppressed phase separation by enhancing matrix viscosity. The resulting beads exhibited stimuli-responsive degradation and controlled release behavior in response to physiological ionic strength. Dense alginate networks delayed ion exchange and prolonged structural integrity, while elevated external ionic conditions triggered rapid disintegration and immediate payload release. This simple and scalable system offers a biocompatible platform for the oral delivery of lipophilic active compounds without the need for surfactants or complex fabrication steps.

摘要

由于疏水性化合物的水溶性差以及与传统表面活性剂基乳液相关的潜在毒性,口服递送疏水性化合物仍然具有挑战性。为了解决这些问题,我们提出了一种无表面活性剂的封装策略,使用电喷雾藻酸盐水凝胶珠来稳定和可控地递送疏水性油。通过超声处理将疏水性化合物分散在不含表面活性剂的高粘度藻酸盐溶液中,形成动力学稳定的水包油分散体。这些混合物被电喷雾到氯化钙浴中,产生单分散的水凝胶珠。较高的藻酸盐浓度通过提高基质粘度改善了液滴的球形度并抑制了相分离。所得珠子在生理离子强度下表现出刺激响应性降解和控释行为。致密的藻酸盐网络延迟了离子交换并延长了结构完整性,而外部离子条件的升高触发了快速崩解和立即释放有效载荷。这个简单且可扩展的系统为口服递送亲脂性活性化合物提供了一个生物相容性平台,无需表面活性剂或复杂的制造步骤。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8f96/12349423/e6e071c2815c/polymers-17-02098-sch001.jpg

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