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DOI 10.1016/j.etap.2016.01.015

Медицинская библиотека · Environmental toxicology and pharmacology · 2016

Bisphosphonates: Pharmacokinetics, bioavailability, mechanisms of action, clinical applications in children, and effects on tooth development.

Soares Ana Prates, do Espírito Santo Renan Fernandes, Line Sérgio Roberto Peres, Pinto Maria das Graças Farias, Santos Pablo de Moura, Toralles Maria Betânia Pereira, do Espírito Santo Alexandre Ribeiro

СтатьяПоддержка исследования: вне правительства СШАОбзорПеревод в очереди

Аннотация

Bisphosphonates (BPs) avidly bind to calcium crystals and inhibit osteoclastic bone resorption, making them useful for treatment of skeletal disorders such as osteoporosis, Paget's disease, osteogenesis imperfecta and metastatic bone diseases. BPs therapeutically act by causing toxic effects on osteoclasts or interfering with specific intracellular pathways in those cells. BPs that possess nitrogen in their composition are called nitrogen-containing BPs (NBPs) and include alendronate, pamidronate, risedronate, ibandronate, and zoledronate. Simple BPs or non-NBPs do not have nitrogen in their composition, include etiodronate and clodronate, and were the first to be tested in animals and clinically used. Because BPs may be administered to pregnant women or children during deciduous and permanent teeth development, it is expected that they might disturb tooth eruption and development. A review of current literature on pharmacokinetics, bioavailability, mechanisms of action, and clinical applications of BPs in children, and their effects on tooth eruption and development is presented.

Для цитирования: Soares Ana Prates, do Espírito Santo Renan Fernandes, Line Sérgio Roberto Peres, Pinto Maria das Graças Farias, Santos Pablo de Moura, Toralles Maria Betânia Pereira, do Espírito Santo Alexandre Ribeiro. Bisphosphonates: Pharmacokinetics, bioavailability, mechanisms of action, clinical applications in children, and effects on tooth development.. Environmental toxicology and pharmacology. 2016. DOI: 10.1016/j.etap.2016.01.015.

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