CIBER de Bioingeniería, Biomateriales y Nanomedicina, CIBER-BBN, Spain; University Hospital La Paz-IdiPAZ, Paseo de la Castellana 261, 28046 Madrid, Spain.
School of Pharmacy and Pharmaceutical Sciences, Trinity College Dublin, The University of Dublin, College Green, Dublin 2, Ireland; Tissue Engineering Research Group, Dept. of Anatomy, Royal College of Surgeons in Ireland, 123 St Stephen's Green, Dublin 2, Ireland; Advanced Materials and Bioengineering Research (AMBER) Centre, CRANN Institute, Trinity College Dublin, Dublin 2, Ireland.
Acta Biomater. 2017 Oct 1;61:54-65. doi: 10.1016/j.actbio.2017.08.010. Epub 2017 Aug 8.
Here we report a composite system based on fibrin hydrogels that incorporate in their structure near-infrared (NIR) responsive nanomaterials and thermosensitive liposomes (TSL). Polymerized fibrin networks entrap simultaneously gold-based nanoparticles (NPs) capable of transducing NIR photon energy into heat, and lysolipid-incorporated TSL (LTSL) loaded with doxorubicin hydrochloride (DOX). NIR irradiation of the resulting hydrogels (referred to as "lipogels") with 808nm laser light increased the temperature of the illuminated areas, leading to the release of the liposomal cargo. Levels of DOX that release from the "smart" composites were dependent on the concentration of NIR nanotransducers loaded in the lipogel, the intensity of the electromagnetic energy deposited and the irradiation regime. Released DOX retained its bioactivity, as shown in cultures of epithelial carcinoma cells. Finally, the developed drug delivery platform was refined by using NIR-photoabsorbers based on copper sulfide NPs to generate completely biodegradable composites as well as through the incorporation of cholesterol (Ch) in LTSL formulation, which lessens leakiness of the liposomal cargo at physiological temperature. This remotely controlled system may suit well for those therapies that require precise control over the dose of delivered drug in a defined spatiotemporal framework.
Hydrogels composed of fibrin embedding nanoparticles responsive to near infrared (NIR) energy and thermosensitive liposomes loaded with doxorubicin hydrochloride (DOX), were prepared by in situ polymerization. NIR-light irradiation of these constructs, referred to as "NIR responsive lipogels", results in the controlled release of DOX to the surrounding medium. This technology may use fully degradable components and can preserve the bioactivity of liposomal cargo after remote triggering to finely regulate the dose and bioavailability of delivered payloads. NIR responsive lipogels technology overcomes the limitations of drug release systems based on the combination of liposomes and degradable polymeric materials, which in many cases lead to insufficient release at therapy onset or to overdose during high degradation period.
在此,我们报告了一种基于纤维蛋白水凝胶的复合体系,该体系在其结构中同时包含近红外(NIR)响应纳米材料和热敏脂质体(TSL)。聚合的纤维蛋白网络同时捕获能够将 NIR 光子能量转化为热能的基于金的纳米颗粒(NPs)和载有盐酸多柔比星(DOX)的含有溶酶体的 TSL(LTSL)。用 808nm 激光对所得水凝胶(称为“脂质凝胶”)进行 NIR 照射会增加照射区域的温度,从而导致脂质体货物的释放。从“智能”复合材料中释放的 DOX 水平取决于负载在脂质凝胶中的 NIR 纳米转导物的浓度、沉积的电磁能的强度和辐照方案。释放的 DOX 保留其生物活性,如上皮癌细胞培养物所示。最后,通过使用基于硫化铜 NPs 的近红外光吸收剂来开发完全可生物降解的复合材料,并通过在 LTSL 配方中加入胆固醇(Ch)来改进所开发的药物输送平台,这可以减少在生理温度下脂质体货物的渗漏。这种远程控制的系统可能非常适合那些需要在定义的时空框架内精确控制递药剂量的治疗方法。
由对近红外(NIR)能量有响应的纳米颗粒和负载盐酸多柔比星(DOX)的热敏脂质体组成的水凝胶,通过原位聚合制备。将这些结构物(称为“NIR 响应脂质凝胶”)进行 NIR 光照会导致 DOX 向周围介质的受控释放。这项技术可以使用完全可降解的成分,并在远程触发后保留脂质体货物的生物活性,以精细调节递药的剂量和生物利用度。NIR 响应脂质凝胶技术克服了基于脂质体和可降解聚合物材料组合的药物释放系统的局限性,在许多情况下,这些系统在治疗开始时导致释放不足或在高降解期导致过量。