Tissue Engineering And Nanotheranostics

(Steven Felgate) #1
b2815 Tissue Engineering and Nanotheranostics “9.61x6.69”

236 Tissue Engineering and Nanotheranostics


probes and biocompatible ligands for specific therapies. For drug


delivery, drug molecules can be encapsulated through the interior


pockets of dendrimers via non­covalent interactions such as electro­


static, hydrophobic, and hydrogen­bond interactions, while drug


molecules can also be conjugated by the surface functionalities via


covalent linkages. Additionally, the cationic dendrimers mainly includ­


ing polyamidoamine and poly(propyleneimine) with abundant tertiary


amine groups on the surface can efficiently condense nucleic acids into


nanomaterials for gene delivery.^1 31–137


2.4. Polymeric Micelle


In recent years, amphiphilic block copolymers forming self­assembled


micellar structure have gained much attention for their application in


drug delivery.138,139 The polymeric micelle has a hydrophobic core con­


sisting of polymer tails and hydrophilic head groups. The micelles are


formed through a process of self­assembly that occurs in a concentration­


dependent manner, referred to as critical micelle concentration. Like


other nanocarriers, the micelle used for drug delivery can improve the


drug tissue distribution and reduce off­target cytotoxicity. The fol­


lowing describes some typical micelles. Poloxamer (trade name


Pluronics) consists of a central poly(propylene oxide) (PPO) block


forming hydrophobic core that is flanked on both sides by two hydro­


philic chains of poly(ethylene oxides) (PEO) forming hydrophilic


corona, yielding a structure of (PEO)a–(PPO)b–(PEO). Poly(lactic)


acid (PLA), approved by the FDA, is used up in citric acid cycle to


produce water and carbon dioxide. In order to improve the weak


hydrophilicity of PLA, copolymerization of PEG–PLA was developed


for the self­assembly of micelles in water with the size range of


10–100 nm.140,141 The clinically approved micellar preparation of


paclitaxel, Genexol­PM has mPEG–PLA as the micelle­forming poly­


mer.142,143 Another class of amphiphilic polyester polymers, PEGy­


lated poly(caprolactone) (PEG–PCL) is an ideal candidate for drug


delivery with its amphiphilic property and ease to synthesis, and


exhibits good biocompatibility, biodegradability and low toxicity pro­


file.^1 44–146 PEG–lipid copolymers are the same as other diblock

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