Continuous inkjet printing of enalapril maleate onto orodispersible film formulations

التفاصيل البيبلوغرافية
العنوان: Continuous inkjet printing of enalapril maleate onto orodispersible film formulations
المؤلفون: Dominique Jasmin Lunter, Joerg Breitkreutz, Yasmin Thabet
المصدر: International journal of pharmaceutics. 546(1-2)
سنة النشر: 2017
مصطلحات موضوعية: Macrogol, Recrystallization (geology), Materials science, Drug Compounding, Pharmaceutical Science, Administration, Oral, 02 engineering and technology, 030226 pharmacology & pharmacy, Dosage form, Polyethylene Glycols, 03 medical and health sciences, 0302 clinical medicine, Enalapril, Inkjet printing, Antihypertensive Agents, Active ingredient, Dosage Forms, Inkwell, Ethanol, Methanol, Water, Continuous manufacturing, 021001 nanoscience & nanotechnology, Drug Combinations, Hydrochlorothiazide, Chemical engineering, Enalapril Maleate, Solvents, Printing, Ink, 0210 nano-technology
الوصف: Piezoelectric inkjet printing onto orodispersible films (ODFs) was proven to be a successful technique applying flexible doses of active pharmaceutical ingredients (APIs) onto edible substrates. The reported API printing and ODF production was conducted in a non-continuous production approach. Within this study, drug-free and hydrochlorothiazide (HCT) containing ODFs should be imprinted in-line with enalapril maleate (EM) ink during continuous ODF production. Macrogol inks based on various solvents and solvent-water mixtures were developed providing dynamic viscosities from 7 to 17 mPa*s. Water based inks contained 1.25%, methanol based inks up to 10% EM. Both inks could be printed (500-1000 Hz) during continuous ODF production. No EM recrystallization was observed for water-based inks. Mechanical properties were not affected by drug printing using various firing frequencies. ODF imprinted with water-based EM inks contained 0.04 mg EM/6 cm2. EM amount can be increased to a paediatric therapeutic dose of 0.5 mg EM utilizing methanol-based inks. These inks were successfully printed onto HCT ODFs resulting in a therapeutically relevant fixed-dose combination. No EM migration into the HCT layer could be observed. In conclusion, it was feasible to print EM doses onto drug-free and HCT ODFs during an in-line continuous manufacturing process.
تدمد: 1873-3476
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6e195e9c36bd2d7d1123018f0f252551
https://pubmed.ncbi.nlm.nih.gov/29753906
حقوق: CLOSED
رقم الأكسشن: edsair.doi.dedup.....6e195e9c36bd2d7d1123018f0f252551
قاعدة البيانات: OpenAIRE