TY - JOUR
T1 - High-density lipoproteins for therapeutic delivery systems
AU - Kannan Mutharasan, R.
AU - Foit, Linda
AU - Shad Thaxton, C.
N1 - Funding Information:
For financial support we thank the Howard Hughes Medical Institute (HHMI) for a Physician Scientist Early Career Award, the Department of Defense/Air Force Office of Scientific Research (FA95501310192 and FA9550-11-1-0275), the National Institutes of Health/National Cancer Institute (U54CA151880 and R01CA167041), and the Dixon Translational Grants Initiative through the Northwestern University Clinical and Translational Sciences Institute.
Publisher Copyright:
© The Royal Society of Chemistry 2016.
PY - 2015
Y1 - 2015
N2 - High-density lipoproteins (HDL) are a class of natural nanostructures found in the blood and are composed of lipids, proteins, and nucleic acids (e.g. microRNA). Their size, which appears to be well-suited for both tissue penetration/retention as well as payload delivery, long circulation half-life, avoidance of endosomal sequestration, and potential low toxicity are all excellent properties to model in a drug delivery vehicle. In this review, we consider high-density lipoproteins for therapeutic delivery systems. First we discuss the structure and function of natural HDL, describing in detail its biogenesis and transformation from immature, discoidal forms, to more mature, spherical forms. Next we consider features of HDL making them suitable vehicles for drug delivery. We then describe the use of natural HDL, discoidal HDL analogs, and spherical HDL analogs to deliver various classes of drugs, including small molecules, lipids, and oligonucleotides. We briefly consider the notion that the drug delivery vehicles themselves are therapeutic, constituting entities that exhibit "theralivery." Finally, we discuss challenges and future directions in the field.
AB - High-density lipoproteins (HDL) are a class of natural nanostructures found in the blood and are composed of lipids, proteins, and nucleic acids (e.g. microRNA). Their size, which appears to be well-suited for both tissue penetration/retention as well as payload delivery, long circulation half-life, avoidance of endosomal sequestration, and potential low toxicity are all excellent properties to model in a drug delivery vehicle. In this review, we consider high-density lipoproteins for therapeutic delivery systems. First we discuss the structure and function of natural HDL, describing in detail its biogenesis and transformation from immature, discoidal forms, to more mature, spherical forms. Next we consider features of HDL making them suitable vehicles for drug delivery. We then describe the use of natural HDL, discoidal HDL analogs, and spherical HDL analogs to deliver various classes of drugs, including small molecules, lipids, and oligonucleotides. We briefly consider the notion that the drug delivery vehicles themselves are therapeutic, constituting entities that exhibit "theralivery." Finally, we discuss challenges and future directions in the field.
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U2 - 10.1039/c5tb01332a
DO - 10.1039/c5tb01332a
M3 - Article
AN - SCOPUS:84952326597
SN - 2050-7518
VL - 4
SP - 188
EP - 197
JO - Journal of Materials Chemistry B
JF - Journal of Materials Chemistry B
IS - 2
ER -