灵芝复方黄体酮包封优化激素替代和靶向抗癌治疗

IF 4.6 3区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY
RSC Advances Pub Date : 2025-06-20 DOI:10.1039/D5RA02368H
Samar M. Mahgoub, Abdullah S. Alawam, Hassan A. Rudayni, Ahmed A. Allam, Aya Shaban, Esraa Khaled, Aya M. Mokhtar, Sahar Abdel Aleem Abdel Aziz and Rehab Mahmoud
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引用次数: 0

摘要

传统的激素替代疗法(HRT)和激素依赖性癌症治疗面临重大挑战,包括孕激素的生物利用度差、代谢快、不良副作用、靶向效率有限和全身毒性。为了解决这些问题,本研究开发了一种创新的黄体酮-灵芝(灵芝)复合材料,利用灵芝的天然生物活性特性来提高治疗效果。将黄体酮包埋在灵芝基质中制备该复合材料,其载药效率高达98.10%。FTIR、SEM、XRD、UV-Vis等表征手段证实了黄体酮与蘑菇基质的包封和相互作用。体外释放研究显示出持续和可控的释放特征,在48小时内释放了88.25%的黄体酮,而游离黄体酮在2-4小时内快速和完全释放。动力学模型揭示了非菲克扩散机制,表明激素与蘑菇基质之间存在协同作用。体外对MCF-7乳腺癌细胞的细胞毒性实验表明,该复合物具有较强的抗肿瘤活性,IC50为81.11 μg mL−1,显著低于游离孕酮(IC50为123.12 μg mL−1)。分子对接研究表明灵芝酸A(灵芝中的一种生物活性化合物)和孕酮与关键受体(PCL-2、PI3K、PR、ERα)具有较强的结合亲和力,提示其在激素调节和肿瘤抑制中具有潜在的协同作用。抗菌实验表明,该复合材料对革兰氏阳性病原菌无乳链球菌(MIC = 41.60 μ mL−1)和金黄色葡萄球菌(MIC = 52.10 μ mL−1)具有较强的抑菌活性(MBC/MIC <;4)。加速稳定性测试(40±2°C/75±5% RH, 6个月)显示孕酮保留率和缓释率为94%,胶体性能稳定,对细菌和白色念珠菌的抗菌活性损失最小,证实了其稳定性和有效性。这项研究表明,将天然生物活性化合物与合成激素结合起来,进行有针对性的有效治疗是有希望的。黄体酮-灵芝复合材料提供了一种双重作用的方法,将激素调节与抗癌和抗菌特性结合起来,为妇女健康和癌症治疗的新疗法铺平了道路。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Encapsulation of progesterone in reishi mushroom composite for optimized hormone replacement and targeted anticancer therapy

Encapsulation of progesterone in reishi mushroom composite for optimized hormone replacement and targeted anticancer therapy

Conventional hormone replacement therapy (HRT) and hormone-dependent cancer treatments face significant challenges, including poor bioavailability, rapid metabolism, and adverse side effects of progesterone, as well as limited targeting efficiency and systemic toxicity. To address these issues, this study develops an innovative progesterone–reishi mushroom (Ganoderma lucidum) composite, leveraging the natural bioactive properties of reishi mushrooms to enhance therapeutic efficacy. The composite was prepared by encapsulating progesterone within the reishi mushroom matrix, achieving a high loading efficiency of 98.10%. Characterization using FTIR, SEM, XRD, and UV-Vis confirmed successful encapsulation and interaction between progesterone and the mushroom matrix. In vitro release studies demonstrated a sustained and controlled release profile, with 88.25% of progesterone released over 48 hours, compared to the rapid and complete release of free progesterone within 2–4 hours. Kinetic modeling revealed a non-Fickian diffusion mechanism, indicating a synergistic interaction between the hormone and the mushroom matrix. In vitro cytotoxicity assays on MCF-7 breast cancer cells showed that the composite exhibited enhanced anticancer activity, with an IC50 of 81.11 μg mL−1, significantly lower than free progesterone (IC50 = 123.12 μg mL−1). Molecular docking studies highlighted the strong binding affinities of ganoderic acid A (a bioactive compound from reishi mushrooms) and progesterone with key receptors (PCL-2, PI3K, PR, ERα), suggesting potential synergistic effects in hormone regulation and cancer inhibition. Antimicrobial assays revealed the composite's potent activity against Gram-positive pathogens, such as Streptococcus agalactiae (MIC = 41.60 μg mL−1) and Staphylococcus aureus (MIC = 52.10 μg mL−1), with bactericidal effects (MBC/MIC < 4). Accelerated stability testing (40 ± 2 °C/75 ± 5% RH, 6 months) showed >94% progesterone retention, sustained release, stable colloidal properties, and minimal loss of antimicrobial activity against bacteria and Candida albicans, confirming its stability and efficacy. This research demonstrates the promise of combining natural bioactive compounds with synthetic hormones for targeted, effective therapies. The progesterone–reishi mushroom composite offers a dual-action approach, integrating hormonal regulation with anticancer and antimicrobial properties, paving the way for novel treatments in women's health and cancer therapy.

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来源期刊
RSC Advances
RSC Advances chemical sciences-
CiteScore
7.50
自引率
2.60%
发文量
3116
审稿时长
1.6 months
期刊介绍: An international, peer-reviewed journal covering all of the chemical sciences, including multidisciplinary and emerging areas. RSC Advances is a gold open access journal allowing researchers free access to research articles, and offering an affordable open access publishing option for authors around the world.
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