Nanoparticle Formulations of Poly (ADP-ribose) Polymerase Inhibitors for Cancer Therapy

Bijay Singh1,2, Shicheng Yang3,2, Apurva Krishna4,2, Srinivas Sridhar4,3,1,5,2
1Department of Physics, Northeastern University, Boston, MA, United States
2Nanomedicine Innovation Center, Northeastern University, Boston, MA, United States
3Department of Chemical Engineering, Northeastern University, Boston, MA, United States
4Department of Bioengineering, Northeastern University, Boston, MA, United States
5Department of Radiation Oncology, Harvard Medical School, Boston, MA, United States

Tóm tắt

A number of poly(ADP-ribose) polymerase (PARP) inhibitors have been recently approved for clinical use in BRCA mutated and other cancers. However, off-target toxicity of PARP inhibitors and the emergence of drug resistance following prolonged administration of these inhibitors indicate the need for improved methods of drug delivery to the tumors. Nanomedicines based upon nanoparticle formulations of conventional small molecule drugs and inhibitors offer many advantages, such as increased solubility and bioavailability of drugs, reduced toxicity and drug resistance, and improved tissue selectivity and therapeutic efficacy. This review highlights the current trends in formulations of PARP inhibitors developed by nanotechnology approaches and provides an insight into the applications and limitations of these PARP inhibitor nanomedicines for cancer therapies.

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