Nuclear and Energy Research Institute, IPEN-CNEN/SP-University of São Paulo, Av. Prof. Lineu Prestes, No. 2242, Cidade Universitária, São Paulo 05508-000, Brazil; Departamento de Farmacología, Farmacia y Tecnología Farmacéutica, I+D Farma (GI-1645), Facultad de Farmacia, Instituto de Materiales (iMATUS) and Health Research Institute of Santiago de Compostela (IDIS), Universidade de Santiago de Compostela, 15782 Santiago de Compostela, Spain.
Departamento de Farmacología, Farmacia y Tecnología Farmacéutica, I+D Farma (GI-1645), Facultad de Farmacia, Instituto de Materiales (iMATUS) and Health Research Institute of Santiago de Compostela (IDIS), Universidade de Santiago de Compostela, 15782 Santiago de Compostela, Spain.
Int J Biol Macromol. 2023 Jul 1;242(Pt 3):124957. doi: 10.1016/j.ijbiomac.2023.124957. Epub 2023 May 20.
Local treatment of bladder cancer faces several limitations such as short residence time or low permeation through urothelium tissue. The aim of this work was to develop patient-friendly mucoadhesive gel formulations combining gemcitabine and the enzyme papain for improved intravesical chemotherapy delivery. Hydrogels based on two different polysaccharides, gellan gum and sodium carboxymethylcellulose (CMC), were prepared with either native papain or papain nanoparticles (nanopapain) to explore for the first time their use as permeability enhancers through bladder tissue. Gel formulations were characterized regarding enzyme stability, rheological behavior, retention on bladder tissue and bioadhesion, drug release properties, permeation capacity, and biocompatibility. After 90 days of storage, the enzyme loaded in the CMC gels retained up to 83.5 ± 4.9 % of its activity in the absence of the drug, and up to 78.1 ± 5.3 with gemcitabine. The gels were mucoadhesive and the enzyme papain showed mucolytic action, which resulted in resistance against washing off from the urothelium and enhanced permeability of gemcitabine in the ex vivo tissue diffusion tests. Native papain shortened lag-time tissue penetration to 0.6 h and enhanced 2-fold drug permeability All formulations demonstrated pseudoplastic behavior and no irritability. Overall, the developed formulations have potential as an upgraded alternative to intravesical therapy for bladder cancer treatment.
局部治疗膀胱癌面临一些局限性,如驻留时间短或通过尿路上皮组织的渗透低。本工作的目的是开发结合吉西他滨和酶木瓜蛋白酶的患者友好型粘弹性凝胶制剂,以改善腔内化疗的传递。基于两种不同多糖(结冷胶和羧甲基纤维素钠(CMC))的水凝胶,用天然木瓜蛋白酶或木瓜蛋白酶纳米颗粒(纳米木瓜蛋白酶)制备,首次探索它们作为通过膀胱组织的通透性增强剂的用途。凝胶制剂的特征在于酶稳定性、流变行为、在膀胱组织上的保留和生物粘附、药物释放特性、渗透能力和生物相容性。在储存 90 天后,在没有药物的情况下,CMC 凝胶中负载的酶保留了其活性的 83.5±4.9%,而与吉西他滨一起保留了 78.1±5.3%。凝胶具有粘膜粘附性,并且酶木瓜蛋白酶显示出粘液溶解作用,这导致其抵抗从尿路上皮冲洗掉,并增强了吉西他滨在离体组织扩散试验中的渗透性。天然木瓜蛋白酶将组织穿透的滞后时间缩短至 0.6 小时,并将药物渗透性增强 2 倍。所有制剂均表现出假塑性行为,没有刺激性。总的来说,所开发的制剂具有作为膀胱癌治疗的升级腔内治疗替代方案的潜力。