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Excipient-free isoniazid aerosol administration in mice: Evaporation-nucleation particle generation, pulmonary delivery and body distribution Научная публикация

Журнал International Journal of Pharmaceutics
ISSN: 0378-5173 , E-ISSN: 1873-3476
Вых. Данные Год: 2019, Том: 563, Страницы: 101-109 Страниц : 9 DOI: 10.1016/j.ijpharm.2019.03.050
Ключевые слова Aerosol; Pulmonary administration; Isoniazid; Pharmacokinetics; Mice
Авторы Valiulin S.V. 1,2,3 , Onischuk A.A. 1,2,3 , Baklanov A.M. 1,2 , Dubtsov S.N. 1,2 , An'kov S., V 4 , Tolstikova T.G. 2,4 , Plokhotnichenko M.E. 1 , Dultseva G.G. 1,2 , Mazunina P.S. 1
Организации
1 (Данные Web of science) RAS, Voevodsky Inst Chem Kinet & Combust, Novosibirsk 630090, Russia
2 (Данные Web of science) Novosibirsk State Univ, Novosibirsk 630090, Russia
3 (Данные Web of science) Novosibirsk State Pedag Univ, Novosibirsk 630126, Russia
4 (Данные Web of science) RAS, NN Vorozhtsov Novosibirsk Inst Organ Chem, Novosibirsk 630090, Russia

Реферат: Excipient-free isoniazid aerosol formation and pulmonary delivery in mice are studied. An evaporation-nucleation route is used for the generation of isoniazid aerosol. Particle diameters and number concentrations are measured with an aerosol spectrometer consisting of a diffusion battery, condensation chamber, and photoelectric counter. The pulmonary delivery of isoniazid particles is studied in both nose-only (NO) and whole-body (WB) inhalation chambers for the particle mean diameter and number concentration to be 600 nm and 6 x 10(6) cm(-3), respectively. It is found that the rate of drug systemic absorption in the WB chamber is 27% higher than that for the NO one because of an additional consumption of drug orally from the fur in the WB chamber. The particle deposition efficiency epsilon in the mouse respiratory tract is measured as a function of mean diameter. The quantity e is equal to 0.7 for the particle diameter d = 10 nm and decreases to 0.2 with the diameter increasing to 300 nm, and then, at d > 300 nm the deposition efficiency increases with diameter to 0.5 at d = 2000 nm. The bioavailability of the aerosol form of isoniazid (72 +/- 10%) is very close to that for the peroral form (61 +/- 10%).
Библиографическая ссылка: Valiulin S.V. , Onischuk A.A. , Baklanov A.M. , Dubtsov S.N. , An'kov S.,.V. , Tolstikova T.G. , Plokhotnichenko M.E. , Dultseva G.G. , Mazunina P.S.
Excipient-free isoniazid aerosol administration in mice: Evaporation-nucleation particle generation, pulmonary delivery and body distribution
International Journal of Pharmaceutics. 2019. V.563. P.101-109. DOI: 10.1016/j.ijpharm.2019.03.050 WOS Scopus РИНЦ OpenAlex
Даты:
Опубликована в печати: 1 мая 2019 г.
Идентификаторы БД:
Web of science: WOS:000466146400011
Scopus: 2-s2.0-85063754525
РИНЦ: 38723189
OpenAlex: W2924313462
Цитирование в БД:
БД Цитирований
Web of science 12
Scopus 8
OpenAlex 9
Альметрики: