Rupel Katia, Fanfoni Lidia, Dus Jacopo, Tommasini Martina, Porrelli Davide, Medagli Barbara, Canfora Federica, Adamo Daniela, Di Lenarda Roberto, Ottaviani Giulia, Biasotto Matteo
Department of Medical, Surgical and Health Sciences, University of Trieste, Strada di Fiume 447, 34149 Trieste, Italy.
Department of Life Sciences, University of Trieste, Via Alexander Fleming 31, 34127 Trieste, Italy.
Curr Issues Mol Biol. 2024 Dec 17;46(12):14244-14258. doi: 10.3390/cimb46120853.
The development of anticancer diagnostic and therapeutic strategies is of crucial importance to improve efficacy and therapeutic specificity. Here, we describe the synthesis and characterization of fluorescent self-assembling nanomicelles (NMs) based on a biocompatible polysaccharide (cellulose, CE) functionalized with a tetraphenyl ethylene derivative (TPEHy) and loaded with Doxorubicin (DOX) with aggregation-induced emission (AIE) properties and pH-dependent drug release. We obtained CE-TPEHy-NMs with an average diameter of 60 ± 17 nm for unloaded NMs and 86 ± 25 nm for NMs loaded with DOX, respectively. Upon testing different conditions, we obtained an encapsulation efficiency of 86% and a loading capacity of 90%. A controlled dialysis experiment showed that the release of DOX after 48 h is minimal at pH 7.4 (11%), increasing at pH 6.5 (50%) and at its maximum at pH 4.5 (80%). The cytotoxicity of blank and loaded CE-TPEHy-NMs at increasing concentrations and different pH conditions was tested on a MG-63 human osteosarcoma cell line. Based on viability assays at pH 7.4, neither unloaded nor loaded CE-TPEHy-NMs exerted any inhibition on cell proliferation. At pH 6.5, proliferation inhibition significantly increased, confirming the pH-dependent release. We characterized and studied the performance of CE-based amphiphilic, biocompatible NMs for controlled drug release in acidic conditions, such as tumor microenvironments. Further studies are required to optimize their synthesis process and to validate their antitumoral properties in vivo.
抗癌诊断和治疗策略的发展对于提高疗效和治疗特异性至关重要。在此,我们描述了基于用四苯基乙烯衍生物(TPEHy)功能化的生物相容性多糖(纤维素,CE)合成并表征的具有聚集诱导发光(AIE)特性和pH依赖性药物释放的荧光自组装纳米胶束(NMs),并负载了阿霉素(DOX)。我们分别获得了空载纳米胶束平均直径为60±17 nm、负载DOX的纳米胶束平均直径为86±25 nm的CE-TPEHy-NMs。在测试不同条件时,我们获得了86%的包封率和90%的载药量。一项对照透析实验表明,DOX在pH 7.4时48小时后的释放量最小(11%),在pH 6.5时增加(50%),在pH 4.5时达到最大(80%)。在MG-63人骨肉瘤细胞系上测试了空白和负载的CE-TPEHy-NMs在浓度增加和不同pH条件下的细胞毒性。基于pH 7.4时的活力测定,空载和负载的CE-TPEHy-NMs均未对细胞增殖产生任何抑制作用。在pH 6.5时,增殖抑制作用显著增加,证实了pH依赖性释放。我们表征并研究了基于CE的两亲性、生物相容性纳米胶束在酸性条件(如肿瘤微环境)下控制药物释放的性能。需要进一步研究来优化其合成过程并在体内验证其抗肿瘤特性。