Smart nanocarriers for enzyme-activated prodrug therapy

Exogenous enzyme-activated prodrug therapy (EPT) is a potential cancer treatment strategy that delivers non-human enzymes into or on the surface of the cell and subsequently converts a non-toxic prodrug into an active cytotoxic substance at a specific location and time. The development of several pharmacological pairs based on EPT has been the focus of anticancer research for more than three decades. Numerous of these pharmacological pairs have progressed to clinical trials, and a few have achieved application in specific cancer therapies. The current review highlights the potential of enzyme-activated prodrug therapy as a promising anticancer treatment. Different microbial, plant, or viral enzymes and their corresponding prodrugs that advanced to clinical trials have been listed. Additionally, we discuss new trends in the field of enzyme-activated prodrug nanocarriers, including nanobubbles combined with ultrasound (NB/US), mesoscopic-sized polyion complex vesicles (PICsomes), nanoparticles, and extracellular vesicles (EVs), with special emphasis on smart stimuli-triggered drug release, hybrid nanocarriers, and the main application of nanotechnology in improving prodrugs. © 2024 Informa UK Limited, trading as Taylor & Francis Group.

Авторы
Abo Qoura L. , Morozova E. , Ramaa S. , Pokrovsky V.S.
Издательство
Journal of Drug Targeting
Номер выпуска
9
Язык
Английский
Страницы
1029-1051
Статус
Опубликовано
Том
32
Год
2024
Организации
  • 1 Research Institute of Molecular and Cellular Medicine, People’s Friendship University of Russia (RUDN University), Moscow, Russian Federation
  • 2 Blokhin National Medical Research Center of Oncology, Ministry of Health of the Russian Federation, Moscow, Russian Federation
  • 3 Engelhardt Institute of Molecular Biology of the, Russian Academy of Sciences, Moscow, Russian Federation
  • 4 Department of Pharmaceutical Chemistry, Bharati Vidyapeeth’s College of Pharmacy, Mumbai, India
Ключевые слова
clinical trials EPT; Enzyme-activated prodrug; magnetic nanoparticles in EPT; nanobubbles in EPT; nanoprodrug; pharmacokinetics of nanocarriers; PICsomes in EPT
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