Poly(ß‐amino ester)s for DNA delivery

Israel Journal of Chemistry - Tập 45 Số 4 - Trang 477-485 - 2005
Gregory T. Zugates1, Steven R. Little1, Daniel G. Anderson1, Róbert Langer1
1Department of Chemical Engineering, Massachusetts Institute of Technology, 77 Massachusetts Avenue, Building E25‐342, Cambridge, Massachusetts 02139, USA

Tóm tắt

AbstractNucleotide‐based therapeutics have the potential to treat many inherited and acquired diseases. However, for this form of therapy to become clinically successful, safe and efficient delivery vehicles need to be developed. In this article, we review the synthesis, properties, and use of poly(ß‐amino ester)s as vectors for gene delivery. High‐throughput synthesis and screening studies have identified poly(ß‐amino ester)s that can complex DNA and mediate transfection with efficiencies that are superior to the best commercially available polymer‐ and lipid‐based transfection reagents. Structure‐function studies show that high‐molecular‐weight (>10 kDa) amine‐terminated polymers with primary alcohol side chains are the most efficient vectors to date. In vivo, the most effective polymer, C32, delivers plasmid DNA at high levels following intra‐tumor injection, with excellent biocompatibility. Interestingly, C32 inhibits transfection to surrounding muscle tissue, making it a good candidate for local gene therapy. In addition to simple polymer/DNA complexes insoluble microparticles can be formed using poly(ß‐amino ester)s to physically encapsulate DNA and with sizes appropriate for phagocytosis by antigen‐presenting cells. Uptake of these particles by macrophages results in protein expression levels up to 5 orders of magnitude higher than traditional poly(lactic‐co‐glycolic acid) microparticles containing DNA and can be potent stimulators of antigen presenting cells. Furthermore, in vivo delivery of poly(ß‐amino ester) microparticle genetic vaccines leads to an antigen‐specific, immune‐mediated rejection of a lethal tumor dosage. Taken together, these results show that poly(ß‐amino ester)s have broad potential as delivery systems for drug and gene therapies.

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Tài liệu tham khảo

10.1002/jso.20001

10.1128/CMR.11.1.42

Federoff H.J., 1998, Prog. Brain. Res., 117, 503, 10.1016/S0079-6123(08)64035-2

10.1016/S0163-7258(01)00150-4

10.1038/423573a

10.1016/S0169-409X(02)00046-7

Ali M., 2004, FASEB J., 18, 152, 10.1096/fj.03-0346fje

10.1023/A:1016073132320

10.1021/bc970098f

10.1016/S0167-4781(98)00274-7

10.1021/bc025529v

10.1073/pnas.92.16.7297

10.1074/jbc.M105250200

10.1002/(SICI)1097-0290(20000120)67:2<217::AID-BIT11>3.0.CO;2-Q

10.1021/bc0000177

10.1080/096876899294823

10.1016/j.addr.2004.12.005

10.1016/S0168-3659(02)00144-X

10.1016/0003-2697(92)90245-3

10.1016/S0168-9525(00)89051-4

10.1021/bc0200529

10.1016/S0168-3659(97)00248-4

10.1016/S0169-409X(03)00040-1

10.1016/S0168-3659(03)00127-5

10.1021/ja984012k

10.1023/A:1007552007765

10.1021/ja0015388

10.1016/j.ymthe.2004.11.015

10.1021/ja016288p

10.1021/ja034429c

10.1021/bc034067y

10.1002/anie.200351244

10.1073/pnas.0407218101

10.1002/1521-3773(20010504)40:9<1707::AID-ANIE17070>3.0.CO;2-F

10.1146/annurev.immunol.18.1.927

10.1089/hum.1993.4.4-419

10.1089/hum.1996.7.17-2185

10.1242/jcs.103.4.1249

10.1089/10430349950018535

10.1038/82383

10.1080/10611860290007478

Walter E., 2001, Stp. Pharma Sci., 11, 45

10.1038/sj.gt.3301347

Arthur J.F., 1997, Cancer. Gene Ther., 4, 17

10.1016/S0168-3659(01)00413-8

10.1038/ni962

10.1023/A:1007582911958

10.1016/S0168-3659(99)00151-0

10.1111/j.1749-6632.2003.tb06029.x

10.1146/annurev.immunol.21.120601.141040

10.1016/S1074-7613(00)80179-X

10.1073/pnas.0403549101

Little S.R.;Lynn D.M.;Puram S.V.;Langer R. J. Control. Release in press.