Development of 3D-printed subcutaneous implants using concentrated polymer/drug solutions

التفاصيل البيبلوغرافية
العنوان: Development of 3D-printed subcutaneous implants using concentrated polymer/drug solutions
المؤلفون: Camila J. Picco, Emilia Utomo, Andrea McClean, Juan Domínguez-Robles, Qonita Kurnia Anjani, Fabiana Volpe-Zanutto, Peter E. McKenna, Jonathan G. Acheson, Dessislava Malinova, Ryan F. Donnelly, Eneko Larrañeta
المصدر: Picco, C J, Utomo, E, McClean, A, Domínguez-Robles, J, Kurnia Anjani, Q, Volpe-Zanuto, F, McKenna, P E, Acheson, J G, Malinova, D, Donnelly, R F & Larrañeta, E 2023, ' Development of 3D-printed subcutaneous implants using concentrated polymer/drug solutions ', International Journal of Pharmaceutics, vol. 631, 122477 . https://doi.org/10.1016/j.ijpharm.2022.122477
بيانات النشر: Elsevier BV, 2023.
سنة النشر: 2023
مصطلحات موضوعية: Poly(ethylene)glycol, Olanzapine, Implant, Pharmaceutical Science, 3D printing, Sustained delivery, Poly(caprolactone)
الوصف: Implantable drug-eluting devices that provide therapeutic cover over an extended period of time following a single administration have potential to improve the treatment of chronic conditions. These devices eliminate the requirement for regular and frequent drug administration, thus reducing the pill burden experienced by patients. Furthermore, the use of modern technologies, such as 3D printing, during implant development and manufacture renders this approach well-suited for the production of highly tuneable devices that can deliver treatment regimens which are personalised for the individual. The objective of this work was to formulate subcutaneous implants loaded with a model hydrophobic compound, olanzapine (OLZ) using robocasting - a 3D-printing technique. The formulated cylindrical implants were prepared from blends composed of OLZ mixed with either poly(caprolactone) (PCL) or a combination of PCL and poly(ethylene)glycol (PEG). Implants were characterised using scanning electron microscopy (SEM), thermal analysis, infrared spectroscopy, and X-ray diffraction and the crystallinity of OLZ in the formulated devices was confirmed. In vitro release studies demonstrated that all the formulations were capable of maintaining sustained drug release over a period of 200 days, with the maximum percentage drug release observed to be c.a. 60% in the same period.
وصف الملف: application/pdf
تدمد: 0378-5173
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f1dfce83d97b136a59d2d6f1df97969d
https://doi.org/10.1016/j.ijpharm.2022.122477
حقوق: OPEN
رقم الأكسشن: edsair.doi.dedup.....f1dfce83d97b136a59d2d6f1df97969d
قاعدة البيانات: OpenAIRE