4.6 Review

Paclitaxel drug delivery systems

Journal

EXPERT OPINION ON DRUG DELIVERY
Volume 10, Issue 3, Pages 325-340

Publisher

TAYLOR & FRANCIS LTD
DOI: 10.1517/17425247.2013.752354

Keywords

cancer nanotechnology; drug delivery systems; drug formulation; nanomedicine; pharmaceutical nanotechnology; taxanes

Funding

  1. National Basic Research Program of China (973 Program) [2012CB932500]
  2. Shenzhen Bureau of Science Technology Information [JC201005270308A]
  3. National Natural Science Foundation of China [201204024, 81241103, 30900291, 31270019, 51203085]
  4. Program for New Century Excellent Talents in University [NCET-11-0275]
  5. Agency of Science, Technology and Research (A*STAR), Singapore [R-398-000-077-305]
  6. Chinese Ministry of Science and Technology (MOST) [R-398-000-077-305]
  7. NUS FSF [R-397-000-136-731]
  8. FRC [R-397-000-136-112]

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Introduction: Paclitaxel (PTX) is one of the most effective broad-spectrum chemotherapeutic agents in the treatment of cancers. However, its clinical application has been limited due to its poor water solubility. Its current clinical administration uses the adjuvant of serious side effects and has undesired pharmacokinetics and biodistribution. There is, thus, a need for the development of alternate drug delivery systems of PTX to enhance its solubility, permeability and stability and further to promote a sustained, controlled and targeted delivery that will increase its therapeutic effects and reduce its side effects. Areas covered: This review is focused on recent developments of the various PTX delivery systems such as prodrugs, micelles, liposomes, solid lipid nanoparticles, nanoparticles of biodegradable polymers, dendrimers, nanohydrogels, as well as PTX-eluting stents. Expert opinion: Pharmaceutical nanotechnology can provide solutions to solve the problems encountered in drug formulation and drug delivery and may change the way drugs are made. The various nanocarriers could have high efficiency in drug encapsulation and cellular uptake, escape from elimination by microphages due to their appropriate size and surface modification and realize with ligand conjugation-targeted delivery.

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