Academic Journal

Platinum pharmacokinetics in mice following inhalation of cisplatin dry powders with different release and lung retention properties

التفاصيل البيبلوغرافية
العنوان: Platinum pharmacokinetics in mice following inhalation of cisplatin dry powders with different release and lung retention properties
المؤلفون: Levet, Vincent, Merlos, Romain, Rosiere, Rémi, Amighi, Karim, Wauthoz, Nathalie
المصدر: International journal of pharmaceutics, 517
سنة النشر: 2017
المجموعة: DI-fusion : dépôt institutionnel de l'Université libre de Bruxelles (ULB)
مصطلحات موضوعية: Sciences pharmaceutiques, Cisplatin, Controlled release, Dry powder for inhalation, Lung cancer chemotherapy, Lung retention, Solid lipid microparticles, Stealth formulation
الوصف: Pharmacokinetics of cisplatin administered by the pulmonary route were established in mice using dry powders inhaler (DPI) formulations showing immediate (F1) and controlled release (CR, solid lipid microparticles) in vitro, without (F2) or with PEGylated excipients (F3, F4). Formulation administration was realized using dry powder blends (correspondingly named thereafter F1B to F4B) able to reproducibly deliver particles in vivo using a DP-4M Dry Powder Insufflator™. Their platinum pharmacokinetics were established over 48 h in lungs, total blood and non-target organs vs. IV and endotracheal nebulization (EN). EN and F1B were rapidly distributed from the lungs (t1/2 i 2.6 and 5.0 min). F2B was eliminated in ∼1 h (t1/2 i 9.0 min). F3B lung retention was sustained for ∼7 h (t1/2 i 59.9 min), increasing lung AUC 11-, 4- and 3-fold vs. IV, F1B and F2B. Total blood tmax were higher and AUC and Cmax lower using the pulmonary route vs. IV. Kidney Cmax was reduced 6-, 2- and 3-fold for F1B, F2B and F3B. AUC in kidneys were 2- to 3-fold lower for F1B and F2B vs. IV but comparable for IV vs. F3B, probably because of kidney saturation. PEGylated solid lipid microparticles provided cisplatin particles with interesting lung retention and CR properties. ; SCOPUS: ar.j ; info:eu-repo/semantics/published
نوع الوثيقة: article in journal/newspaper
وصف الملف: 1 full-text file(s): application/pdf
اللغة: English
ردمك: 978-85-00-72467-1
85-00-72467-6
Relation: uri/info:doi/10.1016/j.ijpharm.2016.12.037; uri/info:pii/S0378517316311796; uri/info:scp/85007246762; uri/info:ulb-repo/set/1; https://dipot.ulb.ac.be/dspace/bitstream/2013/239521/3/Elsevier_223148.pdf; http://hdl.handle.net/2013/ULB-DIPOT:oai:dipot.ulb.ac.be:2013/239521
الاتاحة: http://hdl.handle.net/2013/ULB-DIPOT:oai:dipot.ulb.ac.be:2013/239521
https://dipot.ulb.ac.be/dspace/bitstream/2013/239521/3/Elsevier_223148.pdf
رقم الانضمام: edsbas.AF330E94
قاعدة البيانات: BASE
الوصف
ردمك:9788500724671
8500724676