Chitosan-functionalized antelope horn particles as Pickering stabilizers: enhancement of thermal stabilization and in vitro release of volatile oil from Acorus tatarinowii Schott

IF 6.5 Q1 CHEMISTRY, APPLIED
Xiaoxiao Lin , Fei Luan , Xiaofei Zhang , Dongyan Guo , Bingtao Zhai , Liang Feng , Yajun Shi , Junbo Zou
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Abstract

Acorus tatarinowii Schott volatile oil (ATVO) exhibits significant pharmacological activity but undergoes oxidative decomposition under thermal conditions, reducing active component content and formulation stability. This study introduced Pickering emulsion technology to enhance the antioxidant capacity of ATVO and the stability of solid preparations. Antelope horn (AH) powder, derived from Lingzhu Powder, is pharmacologically active and physically stable; however, it is highly hydrophilic and thus unsuitable as a stabilizer. Through chitosan modification, the contact angle of AH was increased from 62.8° to 87.3°, enabling it to function as an effective Pickering stabilizer. A high-speed shear emulsification method was used to construct Pickering emulsions stabilized by modified AH. Under thermal stress at 60 °C, the Pickering emulsion group showed significantly lower peroxide value and malondialdehyde content compared to free ATVO. GC–MS analysis confirmed a superior stability of volatile components in the emulsion. In vitro dissolution tests in artificial gastric/intestinal fluids demonstrated that the emulsion released ATVO faster and more sustainably over 48 h. In artificial intestinal fluid, the cumulative release ratios of α-asarone and β-asarone reached 66.25 % and 91.32 %, respectively, which were 1.43 and 1.26 times those of ATVO group. This is attributed to the interfacial barrier effect of chitosan-modified AH particles. Chitosan surface modification effectively regulates the interfacial properties of AH, and the resulting Pickering emulsion enhances the thermal stability and dissolution rate of ATVO.

Abstract Image

壳聚糖功能化的羚羊角颗粒作为皮克林稳定剂:增强油梨挥发油的热稳定性和体外释放
石竹桃挥发油(ATVO)具有显著的药理活性,但在高温条件下会发生氧化分解,降低了有效成分的含量和配方的稳定性。为了提高ATVO的抗氧化能力和固体制剂的稳定性,本研究引入了Pickering乳化技术。羚角散是由灵珠散衍生而来,具有药理活性和物理稳定性;然而,它是高度亲水的,因此不适合作为稳定剂。壳聚糖改性后,AH的接触角由62.8°增加到87.3°,使其成为有效的Pickering稳定剂。采用高速剪切乳化法制备了改性氢氧化钠稳定的皮克林乳剂。60℃热应激下,皮克林乳剂组过氧化值和丙二醛含量显著低于游离ATVO。气相色谱-质谱分析证实该乳液中挥发性成分具有良好的稳定性。体外溶出试验表明,乳剂在人工胃液/肠液中释放ATVO的速度更快,持续时间超过48 h。在人工肠液中,α-细辛酮和β-细辛酮的累积释放率分别达到66.25%和91.32%,分别是ATVO组的1.43和1.26倍。这归因于壳聚糖修饰的AH颗粒的界面屏障效应。壳聚糖表面改性有效调节了AH的界面性能,制备的Pickering乳液提高了ATVO的热稳定性和溶解速率。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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CiteScore
8.70
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