Microfluidic formulation, cryoprotection and long-term stability of paclitaxel-loaded π electron-stabilized polymeric micelles

被引:1
作者
Mihyar, Rahaf [1 ]
Shalmani, Armin Azadkhah [1 ]
Wildt, Viktor [1 ]
Sheybanifard, Maryam [1 ]
Wang, Alec [1 ]
May, Jan-Niklas [1 ]
Shahzad, Saba [2 ]
Buhl, Eva Miriam [3 ]
Ruetten, Stephan [3 ]
Behrens, Diana [4 ]
Waltherd, Wolfgang [4 ]
Tiboni, Mattia [5 ]
Casettari, Luca [5 ]
Buyel, Johannes F. [6 ]
Rijcken, Cristianne J. F. [7 ]
Hennink, Wim E. [8 ]
von Stillfried, Saskia [9 ]
Kiessling, Fabian [1 ]
Shi, Yang [1 ]
Metselaar, Josbert M. [1 ]
Lammers, Twan [1 ]
Pena, Quim [1 ]
机构
[1] RWTH Aachen Univ Hosp, Inst Expt Mol Imaging, Forckenbeckstr 55, D-52074 Aachen, Germany
[2] Forschungszentrum Julich, Ernst Ruska Ctr Microscopy & Spect Electrons ER C, Wilhelm Johnen Str, D-52428 Julich, Germany
[3] RWTH Aachen Univ Hosp, Inst Pathol, Electron Microscopy Facil, Pauwelsstr 30, D-52074 Aachen, Germany
[4] Expt Pharmacol & Oncol GmbH, Robert Roessle Str 10, D-13125 Berlin, Germany
[5] Univ Urbino Carlo Bo, Dept Biomol Sci, Via Cale Suore 2-4, I-61029 Urbino, PU, Italy
[6] Univ Nat Resources & Life Sci BOKU, Inst Bioproc Sci & Engn IBSE, Dept Biotechnol, Muthgasse 18, A-1190 Vienna, Austria
[7] Cristal Therapeut, Oxfordlaan 55, NL-6229 EV Maastricht, Netherlands
[8] Univ Utrecht, Utrecht Inst Pharmaceut Sci, Fac Sci, Dept Pharmaceut, NL-3508 TB Utrecht, Netherlands
[9] RWTH Aachen Univ Hosp, Inst Pathol, Pauwelsstr 30, D-52074 Aachen, Germany
基金
欧洲研究理事会;
关键词
Nanomedicine; Polymeric micelles; Cryoprotectants; Microfluidics; Flow manufacturing; NANOPARTICLES; LYOPHILIZATION; DELIVERY; STORAGE;
D O I
10.1016/j.jconrel.2024.08.041
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Controlled manufacturing and long-term stability are key challenges in the development and translation of nanomedicines. This is exemplified by the mRNA-nanoparticle vaccines against COVID-19, which require (ultra-) cold temperatures for storage and shipment. Various cryogenic protocols have been explored to prolong nano-medicine shelf-life. However, freezing typically induces high mechanical stress on nanoparticles, resulting in aggregation or destabilization, thereby limiting their performance and application. Hence, evaluating the impact of freezing and storing on nanoparticle properties already early-on during preclinical development is crucial. In the present study, we used prototypic pi electron-stabilized polymeric micelles based on mPEG-b-p(HPMAm-Bz) b-p(HPMAm-Bz) block copolymers to macro- and microscopically study the effect of different cryoprotective excipients on nanoformulation properties like size and size distribution, as well as on freezing-induced aggregation phenomena via in-situ freezing microscopy. We show that sucrose, unlike trehalose, efficiently cryoprotected paclitaxelloaded micelles, and we exemplify the impact of formulation composition for efficient cryoprotection. We finally establish microfluidic mixing to formulate paclitaxel-loaded micelles with sucrose as a cryoprotective excipient in a single production step and demonstrate their stability for 6 months at-20 degree celsius. The pharmaceutical properties and preclinical performance (in terms of tolerability and tumor growth inhibition in a patient-derived triple-negative breast cancer xenograft mouse model) of paclitaxel-loaded micelles were successfully cryopreserved. Together, our efforts promote future pharmaceutical development and translation of pi electron- stabilized polymeric micelles, and they illustrate the importance of considering manufacturing and storage stability issues early-on during nanomedicine development.
引用
收藏
页码:614 / 626
页数:13
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