Polybasic nanogels for intracellular co-delivery of paclitaxel and carboplatin: a novel approach to ovarian cancer therapy.

Angela M Wagner, Olivia L Lanier, Ani Savk, Nicholas A Peppas
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Abstract

Ovarian cancer is one of the leading causes of cancer-related deaths in women, with limited progress in treatments despite decades of research. Common treatment protocols rely on surgical removal of tumors and chemotherapy drugs, such as paclitaxel and carboplatin, which are capable of reaching cancer cells throughout the body. However, the effectiveness of these drugs is often limited due to toxic reactions in patients, nonspecific drug distribution affecting healthy cells, and the development of treatment resistance. In this study, we introduce a polybasic nanogel system composed of poly(diethylaminoethyl methacrylate-co-cyclohexyl methacrylate)-g-poly(ethylene glycol) designed for the targeted co-delivery of paclitaxel and carboplatin directly to ovarian cancer cells. These nanogel systems can respond to the cellular microenvironment to achieve controlled, on-demand drug release, reducing off-target effects and enhancing therapeutic uptake. Additionally, we investigated nanoparticle degradation and controlled drug release as a function of various crosslinkers, including tetraethylene glycol dimethacrylate, bis(2-methacryloyl)oxyethyl disulfide, poly(lactic acid)-b-poly(ethylene glycol)-b-poly(lactic acid)dimethacrylate, and polycaprolactone dimethacrylate. Our results, using OVCAR-3 human ovarian cancer cells, demonstrated that this dual-delivery system outperformed free drugs in inducing cancer cell death, representing a promising advance in the field of nanoparticle-based therapies for ovarian cancer. By loading two chemotherapeutic agents into a single, environmentally responsive particle, this approach shows the potential to overcome common resistance mechanisms and achieve more effective tumor suppression. In summary, by delivering chemotherapy more precisely, it may be possible to enhance therapeutic outcomes while minimizing toxicity and nonspecific drug distribution, ultimately improving patient quality of life.

用于紫杉醇和卡铂细胞内联合给药的多基质纳米凝胶:卵巢癌治疗的新方法。
卵巢癌是女性癌症相关死亡的主要原因之一,尽管进行了数十年的研究,但治疗进展有限。常见的治疗方案依赖于手术切除肿瘤和化疗药物,如紫杉醇和卡铂,这些药物能够到达全身的癌细胞。然而,由于患者的毒性反应、影响健康细胞的非特异性药物分布以及治疗耐药性的发展,这些药物的有效性往往受到限制。在这项研究中,我们介绍了一种由聚(二乙基氨基乙基甲基丙烯酸酯-共甲基丙烯酸环己基)-g-聚乙二醇组成的聚碱纳米凝胶体系,旨在将紫杉醇和卡铂直接靶向递送到卵巢癌细胞。这些纳米凝胶系统可以响应细胞微环境,实现受控的按需药物释放,减少脱靶效应,增强治疗吸收。此外,我们还研究了纳米颗粒降解和控制药物释放作为各种交联剂的功能,包括四乙二醇二甲丙烯酸酯、双(2-甲基丙烯酰)氧乙基二硫化物、聚(乳酸)-b-聚(乙二醇)-b-聚(乳酸)二甲丙烯酸酯和聚己内酯二甲丙烯酸酯。我们使用OVCAR-3人卵巢癌细胞的研究结果表明,这种双重递送系统在诱导癌细胞死亡方面优于免费药物,代表了基于纳米颗粒的卵巢癌治疗领域的一个有希望的进展。通过将两种化疗药物装载到一个单一的环境响应颗粒中,这种方法显示出克服常见耐药机制并实现更有效的肿瘤抑制的潜力。总之,通过更精确地提供化疗,有可能提高治疗效果,同时最大限度地减少毒性和非特异性药物分布,最终改善患者的生活质量。
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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