Tissue Engineering And Nanotheranostics

(Steven Felgate) #1

“9.61x6.69” b2815 Tissue Engineering and Nanotheranostics


Multifunctional Nanomaterials for Cancer Theranostics 241

therapeutic targets through two strategies. The first is to block tumor


suppressor miRNA and the other is to target the genes. Thus, the


miRNA can be delivered to target cells by using targeted nanocarrier


system. siRNA is also utilized in the treatment of cancers. For exam­


ple, siRNA was successfully delivered to cyclin CD­1 to silence the


target in leukocytes by liposomes decorated with monoclonal anti­


bodies.^215 Polymer nanomaterials decorated with the integrin ligand


RGD were utilized to deliver siRNA to endothelial cells during


angiogenesis.^216


3.2. Food and Drug Administration-approved Nanodrugs


Because a large number of powerful evidences suggest that the nano­


carrier for anticancer drug delivery can improve the tissue distribution


of drugs, improve the uptake of drugs in the tumors, enhance the


effect of tumor therapy, and reduce the side effects of drugs, the FDA


has approved nearly 10 kinds of nanoparticle drug formulations.^73 In


1995, Doxil was approved for the therapy of ovarian cancer and sar­


coma. In 1996, DaunoXome was approved for the therapy of sar­


coma. In 2002, Eligard (PLGH­polymer and leuprolide formulation)


was approved for the therapy of late­stage prostate cancer. In 2005,


Abraxane was approved for the therapy of breast cancer. In 2006 and


2007, Oncaspar (PEG­L­asparagine) and Genexol­PM (PLA­PEG


micelle with paclitaxel) were approved for the therapy of acute lymph­


oblastic leukemia and metastatic breast cancer, respectively. Moreover,


nanoparticle­based formulations mainly including many liposomal­


based drugs are in various stages of clinical development to test their


pharmacokinetics and biodistribution profiles. The new drugs of irinote­


can SN­38 in phase I/II to treat colorectal cancer and a liposomal­


based all­trans­retinoic acid (ATRA) tretinoin in phase II to treat


acute promyelocytic leukemia and hormone­refractory prostate can­


cer are underway. EndoTAG­1, PTX embedded in a cationic lipo­


some, is in phase II trials to treat advanced triple­negative breast


cancer and pancreatic cancer. LEP­ETU (liposome­ entrapped pacli­


taxel easy­to­use) as typical another form of PTX, is in phase I/II


trials. Additionally, DOPC is a recently developed neutral liposome

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