Фармакокинетические параметры комплекса цинка с N‑аллилимидазолом
DOI:
https://doi.org/10.18413/rrpharmacology.12.1240Аннотация
Введение: Цинк является эссенциальным микроэлементом, выполняющим хорошо известные физиологические функции. Несмотря на наличие различных солей цинка, новые комплексы цинка с органическими лигандами представляют фармакологический интерес. Фармакокинетические исследования необходимы для выяснения вклада иона цинка и органического лиганда в их биологическую активность.
Материалы и методы: Фармакокинетика компонентов бис(N-аллилимидазол)диацетата цинка (ALL) была изучена на 66 мышах линии BALB/c. Соединение вводили однократно внутрибрюшинно в дозе 25 мг/кг. Образцы крови, головного мозга, печени, поджелудочной железы, почек и селезёнки отбирали через 0; 0,083; 0,25; 0,5; 1; 1,5; 2; 3; 4; 6 и 24 часа, по 6 животных на каждый временной интервал. Количественное определение N-аллилимидазола проводили с использованием валидированного метода ВЭЖХ-МС/МС, а цинка - методом атомно-абсорбционной спектрометрии.
Результаты и обсуждение: Вероятно, в физиологических условиях ALL диссоциирует на N-аллилимидазол и цинк, что приводит к различающимся фармакокинетическим профилям этих компонентов. N-аллилимидазол обнаруживался во всех исследованных тканях, включая головной мозг. Для большинства тканей время достижения максимальной концентрации (Tmax) составляло 0,25 часа, что указывает на быстрое системное распределение. Наиболее высокая концентрация наблюдалась в почках (Cmax 7907,58 мкг/г), что указывает на их участие в выведении лиганда. В печени N-аллилимидазол сохранялся в течение более длительного времени; период полувыведения (T1/2) составлял 14,5 часа, а площадь под фармакокинетической кривой AUC(0-24) - 11168,41 мкг·ч/мл. После коррекции с учётом эндогенного цинка наиболее высокие концентрации цинка выявлялись в печени (60,21 мкг/г), поджелудочной железе (57,52 мкг/г) и селезёнке (54,80 мкг/г).
Заключение: Введение ALL приводило к быстрому системному распределению обоих компонентов. N-аллилимидазол проникал в ткани с высоким кровоснабжением, включая головной мозг и почки, тогда как цинк накапливался в печени, поджелудочной железе и селезёнке. Различия в распределении по тканям и профилях выведения компонентов, наряду с результатами расчётов равновесия, подтверждают полную диссоциацию комплекса in vivo.
Графическая аннотация
Ключевые слова:
цинк, N-аллилимидазол, фармакокинетика, ВЭЖХ-ЭCИ-МС/МС, атомно-абсорбционная спектрометрияБиблиографические ссылки
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