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Design and Synthesis of Cabazitaxel Loaded Core-Shell Mesoporous Silica Nanoparticles with Different Morphologies for Prostate Cancer Therapy.

التفاصيل البيبلوغرافية
العنوان: Design and Synthesis of Cabazitaxel Loaded Core-Shell Mesoporous Silica Nanoparticles with Different Morphologies for Prostate Cancer Therapy.
المؤلفون: Mohanan S; Global Innovative Centre for Advanced Nanomaterials, College of Engineering, Science and Environment, The University of Newcastle, Callaghan, 2308, Australia., Sathish CI; Global Innovative Centre for Advanced Nanomaterials, College of Engineering, Science and Environment, The University of Newcastle, Callaghan, 2308, Australia., Ramadass K; Global Innovative Centre for Advanced Nanomaterials, College of Engineering, Science and Environment, The University of Newcastle, Callaghan, 2308, Australia., Liang M; School of Biomedical Sciences and Pharmacy, College of Health Medicine and Wellbeing, The University of Newcastle, Callaghan, 2308, Australia., Vinu A; Global Innovative Centre for Advanced Nanomaterials, College of Engineering, Science and Environment, The University of Newcastle, Callaghan, 2308, Australia.
المصدر: Small (Weinheim an der Bergstrasse, Germany) [Small] 2024 Sep; Vol. 20 (39), pp. e2303269. Date of Electronic Publication: 2023 Jun 29.
نوع المنشور: Journal Article
اللغة: English
بيانات الدورية: Publisher: Wiley-VCH Country of Publication: Germany NLM ID: 101235338 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1613-6829 (Electronic) Linking ISSN: 16136810 NLM ISO Abbreviation: Small Subsets: MEDLINE
أسماء مطبوعة: Original Publication: Weinheim, Germany : Wiley-VCH, c2005-
مواضيع طبية MeSH: Silicon Dioxide*/chemistry , Nanoparticles*/chemistry , Prostatic Neoplasms*/drug therapy , Prostatic Neoplasms*/pathology , Taxoids*/pharmacology , Taxoids*/chemistry, Humans ; Male ; Porosity ; Cell Line, Tumor ; Particle Size ; PC-3 Cells ; Antineoplastic Agents/pharmacology ; Antineoplastic Agents/chemistry ; Drug Delivery Systems ; Cell Survival/drug effects ; Drug Carriers/chemistry
مستخلص: In this work, the synthesis of core-shell ordered mesoporous silica nanoparticles (CSMS) with tunable particle size and shape through a dual surfactant-assisted approach is demonstrated. By varying the synthesis conditions, including the type of the solvent and the concentration of the surfactant, monodispersed and ordered mesoporous silica nanoparticles with tunable particle size (140-600 nm) and morphologies (hexagonal prism (HP), oblong, spherical, and hollow-core) can be realized. Comparative studies of the Cabazitaxel (CBZ)-loaded HP and spherical-shaped CSMS are conducted to evaluate their drug delivery efficiency to PC3 (prostate cancer) cell lines. These nanoparticles showed good biocompatibility and displayed a faster drug release at acidic pH than at basic pH. The cellular uptake of CSMS measured using confocal microscopy, flow cytometry, microplate reader, and ICP-MS (inductively coupled plasma mass spectrometry) techniques in PC3 cell lines revealed a better uptake of CSMS with HP morphology than its spherical counterparts. Cytotoxicity study showed that the anticancer activity of CBZ is improved with a higher free radical production when loaded onto CSMS. These unique materials with tunable morphology can serve as an excellent drug delivery system and will have potential applications for treating various cancers.
(© 2023 The Authors. Small published by Wiley‐VCH GmbH.)
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فهرسة مساهمة: Keywords: cancer; core shells; drug delivery; mesoporous silica; nanoparticles
المشرفين على المادة: 51F690397J (cabazitaxel)
7631-86-9 (Silicon Dioxide)
0 (Taxoids)
0 (Antineoplastic Agents)
0 (Drug Carriers)
تواريخ الأحداث: Date Created: 20230630 Date Completed: 20240926 Latest Revision: 20240926
رمز التحديث: 20240926
DOI: 10.1002/smll.202303269
PMID: 37386787
قاعدة البيانات: MEDLINE
الوصف
تدمد:1613-6829
DOI:10.1002/smll.202303269