-
1
-
-
0038518258
-
Chemical approaches to triggerable lipid vesicles for drug and gene delivery
-
Guo X, Szoka FC Jr. 2003. Chemical approaches to triggerable lipid vesicles for drug and gene delivery. Acc. Chem. Res. 36:335-41
-
(2003)
Acc. Chem. Res.
, vol.36
, pp. 335-341
-
-
Guo, X.1
Szoka Jr., F.C.2
-
2
-
-
34249820576
-
Multifunctional nanocarriers
-
DOI 10.1016/j.addr.2006.09.009, PII S0169409X06001785, Particulate Nanomedicines
-
Torchilin VP. 2006. Multifunctional nanocarriers. Adv. Drug. Deliv. Rev. 58:1532-55 (Pubitemid 44822608)
-
(2006)
Advanced Drug Delivery Reviews
, vol.58
, Issue.14
, pp. 1532-1555
-
-
Torchilin, V.P.1
-
4
-
-
0347383957
-
Using bioinspired thermally triggered liposomes for high-efficiency mixing and reagent delivery in microfluidic devices
-
DOI 10.1021/ac034850j
-
Vreeland WN, Locascio LE. 2003. Using bioinspired thermally triggered liposomes for high-efficiency mixing and reagent delivery in microfluidic devices. Anal. Chem. 75:6906-11 (Pubitemid 37523591)
-
(2003)
Analytical Chemistry
, vol.75
, Issue.24
, pp. 6906-6911
-
-
Vreeland, W.N.1
Locascio, L.E.2
-
5
-
-
84985609913
-
Vesicleswith a single-Layer and redox-Activemembrane
-
BaumgartnerE, Fuhrhop JH. 1980. Vesicleswith a single-layer and redox-activemembrane. Angew. Chem. Int. Ed. 19:550-51
-
(1980)
Angew. Chem. Int. E.d.
, vol.19
, pp. 550-551
-
-
Baumgartner, E.1
Fuhrhop, J.H.2
-
6
-
-
33845554929
-
Redox active functionally polymerized surfactant vesicles syntheses and characterization
-
Tundo P, Kippenberger DJ, PolitiMJ, Klahn P, Fendler JH. 1982. Redox active functionally polymerized surfactant vesicles. Syntheses and characterization. J. Am. Chem. Soc. 104:5352-58
-
(1982)
J. Am. Chem. Soc.
, vol.104
, pp. 5352-5358
-
-
Tundo, P.1
Kippenberger, D.J.2
Politi, M.J.3
Klahn, P.4
Fendler, J.H.5
-
7
-
-
0346985102
-
Use of conducting electroactive polymers for drug delivery and sensing of bioactive molecules a redox chemistry approach
-
Pernaut J-M, Reynolds JR. 2000. Use of conducting electroactive polymers for drug delivery and sensing of bioactive molecules. A redox chemistry approach. J. Phys. Chem. B 104:4080-90
-
(2000)
J. Phys. Chem.
, vol.B104
, pp. 4080-4090
-
-
Pernaut, J.-M.1
Reynolds, J.R.2
-
8
-
-
77749239896
-
Cucurbituril and cyclodextrin complexes of dendrimers
-
ed. G Wenz, New York Springer
-
Wang W, Kaifer AE. 2009. Cucurbituril and cyclodextrin complexes of dendrimers. In Advances in Polymer Science, vol. 222, ed. G Wenz, pp. 205-35. New York: Springer
-
(2009)
Advances in Polymer Science
, vol.222
, pp. 205-35
-
-
Wang, W.1
Kaifer, A.E.2
-
9
-
-
33845554056
-
Electrically stimulated release of neurotransmitters from a surface an analog of the presynaptic terminal
-
Miller LL, Lau ANK,Miller EK. 1982. Electrically stimulated release of neurotransmitters from a surface. An analog of the presynaptic terminal. J. Am. Chem. Soc. 104:5242-44
-
(1982)
J. Am. Chem. Soc.
, vol.104
, pp. 5242-5244
-
-
Miller, L.L.1
Lau, A.N.K.2
Miller, E.K.3
-
11
-
-
26944439409
-
Redox-driven shaving of dendrimers
-
DOI 10.1039/b506724c
-
OngW, McCarley RL. 2005. Redox-driven shaving of dendrimers. Chem. Commun. 2005:4699-701 (Pubitemid 41475758)
-
(2005)
Chemical Communications
, Issue.37
, pp. 4699-4701
-
-
Ong, W.1
McCarley, R.L.2
-
12
-
-
33751307481
-
Chemically and electrochemically mediated release of dendrimer end groups
-
DOI 10.1021/ma061341l
-
OngW,McCarleyRL. 2006. Chemically and electrochemically mediated release of dendrimer end groups. Macromolecules 39:7295-301 (Pubitemid 44807670)
-
(2006)
Macromolecules
, vol.39
, Issue.21
, pp. 7295-7301
-
-
Ong, W.1
McCarley, R.L.2
-
13
-
-
0034641218
-
Pyrrole-terminated diaminobutane (DAB) dendrimer monolayers on gold: Oligomerization of peripheral groups and adhesion promotion of poly(pyrrole) films [16]
-
DOI 10.1021/ja0010610
-
Noble CO, McCarley RL. 2000. Pyrrole-terminated diaminobutane (DAB) dendrimer monolayers on gold: oligomerization of peripheral groups and adhesion promotion of poly(pyrrole) films. J. Am. Chem. Soc. 122:6518-19 (Pubitemid 30481764)
-
(2000)
Journal of the American Chemical Society
, vol.122
, Issue.27
, pp. 6518-6519
-
-
Noble IV, C.O.1
McCarley, R.L.2
-
14
-
-
37049109052
-
Reversible formation and disruption of micelles by control of the redox state of the surfactant tail group
-
Saji T, Hoshino K, Aoyagui S. 1985. Reversible formation and disruption of micelles by control of the redox state of the surfactant tail group. Chem. Commun. 1985:865-66
-
(1985)
Chem. Commun.
, vol.1985
, pp. 865-866
-
-
Saji, T.1
Hoshino, K.2
Aoyagui, S.3
-
15
-
-
0040171228
-
Reversible formation and disruption of micelles by control of the redox state of the head group
-
Saji T, Hoshino K, Aoyagui S. 1985. Reversible formation and disruption of micelles by control of the redox state of the head group. J. Am. Chem. Soc. 107:6865-68
-
(1985)
J. Am. Chem. Soc.
, vol.107
, pp. 6865-6868
-
-
Saji, T.1
Hoshino, K.2
Aoyagui, S.3
-
16
-
-
0000176317
-
Electroless plating of organic thin films by reduction of nonionic surfactants containing an azobenzene group
-
Saji T, Ebata K, Sugawara K, Liu S, Kobayashi K. 1994. Electroless plating of organic thin films by reduction of nonionic surfactants containing an azobenzene group. J. Am. Chem. Soc. 116:6053-54 (Pubitemid 24981250)
-
(1994)
Journal of the American Chemical Society
, vol.116
, Issue.13
, pp. 6053-6054
-
-
Saji, T.1
Ebata, K.-I.2
Sugawara, K.3
Liu, S.4
Kobayashi, K.5
-
17
-
-
0038740000
-
Electroactive deposits of anthraquinone-attached micelle-and vesicle-forming surfactant assemblies on glassy carbon surfaces
-
Subramanian M, Mandal SK, Bhattacharya S. 1997. Electrochemistry of anthraquinone-attached micelleand vesicle-forming surfactant assemblies on glassy carbon surfaces. Langmuir 13:153-60 (Pubitemid 127591911)
-
(1997)
Langmuir
, vol.13
, Issue.2
, pp. 153-160
-
-
Subramanian, M.1
Mandal, S.K.2
Bhattacharya, S.3
-
18
-
-
0033877826
-
Study of the correlation of the cyclic voltammetric responses of a nonionic surfactant containing an anthraquinone group with the dissolved states
-
DOI 10.1021/la991033z
-
SusanMA, Begum M, Takeoka Y,WatanabeM. 2000. Study of the correlation of the cyclic voltammetric responses of a nonionic surfactant containing an anthraquinone group with the dissolved states. Langmuir 16:3509-16 (Pubitemid 30581085)
-
(2000)
Langmuir
, vol.16
, Issue.7
, pp. 3509-3516
-
-
Susan, Md.A.B.H.1
Begum, M.2
Takeoka, Y.3
Watanabe, M.4
-
19
-
-
8144226997
-
Surface activity and redox behavior of a non-ionic surfactant containing a phenothiazine group
-
DOI 10.1016/j.colsurfb.2004.01.016, PII S0927776504002115
-
Susan M, Ishibashi A, Takeoka Y,Watanabe M. 2004. Surface activity and redox behavior of a non-ionic surfactant containing a phenothiazine group. Colloid Surf. B 38:167-73 (Pubitemid 39473333)
-
(2004)
Colloids and Surfaces B: Biointerfaces
, vol.38
, Issue.3-4 SPEC. ISS.
, pp. 167-173
-
-
Susan, Md.A.B.H.1
Ishibashi, A.2
Takeoka, Y.3
Watanabe, M.4
-
20
-
-
77955355478
-
Tetrathiafulvalene end-functionalized poly(N-isopropylacrylamide): A new class of amphiphilic polymer for the creation of multistimuli responsive micelles
-
Bigot J, Charleux B, Cooke G, Delattre F, Fournier D, et al. 2010. Tetrathiafulvalene end-functionalized poly(N-isopropylacrylamide): a new class of amphiphilic polymer for the creation of multistimuli responsive micelles. J. Am. Chem. Soc. 132:10796-801
-
(2010)
J. Am. Chem. Soc.
, vol.132
, pp. 10796-801
-
-
Bigot, J.1
Charleux, B.2
Cooke, G.3
Delattre, F.4
Fournier, D.5
-
21
-
-
4744339245
-
Control of viscoelasticity using redox reaction
-
DOI 10.1021/ja0467162
-
Tsuchiya K, Orihara Y, Kondo Y, Yoshino N, Ohkubo T, et al. 2004. Control of viscoelasticity using redox reaction. J. Am. Chem. Soc. 126:12282-83 (Pubitemid 39310531)
-
(2004)
Journal of the American Chemical Society
, vol.126
, Issue.39
, pp. 12282-12283
-
-
Tsuchiya, K.1
Orihara, Y.2
Kondo, Y.3
Yoshino, N.4
Ohkubo, T.5
Sakai, H.6
Abet, M.7
-
22
-
-
79954536394
-
Lateral transport of solutes in microfluidic channels using electrochemically generated gradients in redox-Active surfactants
-
Liu X, Abbott NL. 2011. Lateral transport of solutes in microfluidic channels using electrochemically generated gradients in redox-active surfactants. Anal. Chem. 83:3033-41
-
(2011)
Anal. Chem.
, vol.83
, pp. 3033-3041
-
-
Liu, X.1
Abbott, N.L.2
-
23
-
-
51049095142
-
PEG-B-PPS diblock copolymer aggregates for hydrophobic drug solubilization and release: Cyclosporin A as an example
-
Velluto D, Demurtas D, Hubbell JA. 2008. PEG-b-PPS diblock copolymer aggregates for hydrophobic drug solubilization and release: cyclosporin A as an example. Mol. Pharmacol. 5:632-42
-
(2008)
Mol. Pharmacol.
, vol.5
, pp. 632-642
-
-
Velluto, D.1
Demurtas, D.2
Hubbell, J.A.3
-
24
-
-
2342638360
-
Glucose-Oxidase based self-Destructing polymeric vesicles
-
Napoli A, Boerakker MJ, Tirelli N, Nolte RJM, Sommerdijk NAJM, Hubbell JA. 2004. Glucose-oxidase based self-destructing polymeric vesicles. Langmuir 20:3487-91
-
(2004)
Langmuir.
, vol.20
, pp. 3487-3491
-
-
Napoli, A.1
Boerakker, M.J.2
Tirelli, N.3
Nolte, R.J.M.4
Sommerdijk, N.A.J.M.5
Hubbell, J.A.6
-
25
-
-
1542303712
-
Oxidation-Responsive polymeric vesicles
-
Napoli A, Valentini M, Tirelli N, MullerM, Hubbell JA. 2004. Oxidation-responsive polymeric vesicles. Nat. Mater. 3:183-89
-
(2004)
Nat. Mater.
, vol.3
, pp. 183-189
-
-
Napoli, A.1
Valentini, M.2
Tirelli, N.3
MullerM Hubbell, J.A.4
-
26
-
-
0042184381
-
Redox-Responsive liposomal system release of entrapped dye utilizing N,N-Diacylcystine as the functional amphiphile
-
Okabe H, Kamagami S, Kainose H, Ishigami Y. 1991. Redox-responsive liposomal system. Release of entrapped dye utilizing N,N-diacylcystine as the functional amphiphile. Chem. Express 6:315-18
-
(1991)
Chem. Express
, vol.6
, pp. 315-318
-
-
Okabe, H.1
Kamagami, S.2
Kainose, H.3
Ishigami, Y.4
-
27
-
-
0033772657
-
Lipoic acid-Derived amphiphiles for redox-Controlleddna delivery
-
Balakirev M, SchoehnG,Chroboczek J. 2000. Lipoic acid-derived amphiphiles for redox-controlledDNA delivery. Chem. Biol. 7:813-19
-
(2000)
Chem. Biol.
, vol.7
, pp. 813-819
-
-
Balakirev, M.1
Schoehn, G.2
Chroboczek, J.3
-
28
-
-
34547342777
-
Tunable disassembly of micelles using a redox trigger
-
DOI 10.1021/la700981z
-
Ghosh S, Irvin K, Thayumanavan S. 2007. Tunable disassembly of micelles using a redox trigger. Langmuir 23:7916-19 (Pubitemid 47155294)
-
(2007)
Langmuir
, vol.23
, Issue.15
, pp. 7916-7919
-
-
Ghosh, S.1
Irvin, K.2
Thayumanavan, S.3
-
29
-
-
0029175398
-
Measurement of equilibrium midpoint potentials of thiol/disulfide regulatory groups on thioredoxinactivated chloroplast enzymes
-
HutchisonRS, OrtDR, Lester P. 1995. Measurement of equilibrium midpoint potentials of thiol/disulfide regulatory groups on thioredoxinactivated chloroplast enzymes. Methods Enzymol. 252:220-28
-
(1995)
Methods Enzymol.
, vol.252
, pp. 220-228
-
-
Hutchison, R.S.1
Ort, D.R.2
Lester, P.3
-
30
-
-
67749137431
-
Multi-Stimuli sensitive amphiphilic block copolymer assemblies
-
Klaikherd A, Nagamani C, Thayumanavan S. 2009. Multi-stimuli sensitive amphiphilic block copolymer assemblies. J. Am. Chem. Soc. 131:4830-38
-
(2009)
J. Am. Chem. Soc.
, vol.131
, pp. 4830-4838
-
-
Klaikherd, A.1
Nagamani, C.2
Thayumanavan, S.3
-
32
-
-
33646043446
-
Synthesis of reversible shell cross-Linked micelles for controlled release of bioactive agents
-
Li Y, Lokitz BS, Armes SP, McCormick CL. 2006. Synthesis of reversible shell cross-linked micelles for controlled release of bioactive agents. Macromolecules 39:2726-28
-
(2006)
Macromolecules
, vol.39
, pp. 2726-2728
-
-
Li, Y.1
Lokitz, B.S.2
Armes, S.P.3
McCormick, C.L.4
-
33
-
-
74949092148
-
Dual redox responsive assemblies formed from diselenide block copolymers
-
Ma N, Li Y, Xu HP,Wang ZQ, Zhang X. 2010. Dual redox responsive assemblies formed from diselenide block copolymers. J. Am. Chem. Soc. 132:442-43
-
(2010)
J. Am. Chem. Soc.
, vol.132
, pp. 442-443
-
-
Ma, N.1
Li, Y.2
Xu, H.P.3
Wang, Z.Q.4
Zhang, X.5
-
34
-
-
0000334861
-
Redox-Switched molecular aggregates: The first example of vesicle formation from hydrophobic ferrocene derivatives
-
Medina JC, Gay I, Chen Z, Echegoyen L, Gokel GW. 1991. Redox-switched molecular aggregates: the first example of vesicle formation from hydrophobic ferrocene derivatives. J. Am. Chem. Soc. 113:365-66
-
(1991)
J. Am. Chem. Soc.
, vol.113
, pp. 365-366
-
-
Medina, J.C.1
Gay, I.2
Chen, Z.3
Echegoyen, L.4
Gokel, G.W.5
-
35
-
-
0039508990
-
Redox-Switched vesicle formation from two novel, structurally distinct metalloamphiphiles
-
Munoz S, Gokel GW. 1993. Redox-switched vesicle formation from two novel, structurally distinct metalloamphiphiles. J. Am. Chem. Soc. 115:4899-900
-
(1993)
J. Am. Chem. Soc.
, vol.115
, pp. 4899-4900
-
-
Munoz, S.1
Gokel, G.W.2
-
36
-
-
0028912563
-
Control of vesicle formation by chemical switching
-
Munoz S, Abel E, Wang K, Gokel GW. 1995. Control of vesicle formation by chemical switching. Tetrahedron 51:423-34
-
(1995)
Tetrahedron
, vol.51
, pp. 423-434
-
-
Munoz, S.1
Abel, E.2
Wang, K.3
Gokel, G.W.4
-
37
-
-
3442898843
-
Active control of vesicle formation using a redox-active surfactant
-
Sakai H, Imamura H, Kakizawa Y, Abe M, Kondo Y, et al. 1997. Active control of vesicle formation using a redox-active surfactant. Denki Kagaku Oyobi Kogyo 65:669-72
-
(1997)
Denki Kagaku Oyobi Kogyo
, vol.65
, pp. 669-672
-
-
Sakai, H.1
Imamura, H.2
Kakizawa, Y.3
Abe, M.4
Kondo, Y.5
-
38
-
-
0000831675
-
Solution properties of double-tailed cationic surfactants having ferrocenyl groups in their hydrophobic moieties
-
Kakizawa Y, Sakai H, Nishiyama K, Abe M, Shoji H, et al. 1996. Solution properties of double-tailed cationic surfactants having ferrocenyl groups in their hydrophobic moieties. Langmuir 12:921-24 (Pubitemid 126568086)
-
(1996)
Langmuir
, vol.12
, Issue.4
, pp. 921-924
-
-
Kakizawa, Y.1
Sakai, H.2
Nishiyama, K.3
Abe, M.4
Shoji, H.5
Kondo, Y.6
Yoshino, N.7
-
39
-
-
0035951235
-
Electrochemical control of vesicle formation with a double-Tailed cationic surfactant bearing ferrocenyl moieties
-
Kakizawa Y, Sakai H, Yamaguchi A, Kondo Y, Yoshino N, AbeM. 2001. Electrochemical control of vesicle formation with a double-tailed cationic surfactant bearing ferrocenyl moieties. Langmuir 17:8044-48
-
(2001)
Langmuir
, vol.17
, pp. 8044-8048
-
-
Kakizawa, Y.1
Sakai, H.2
Yamaguchi, A.3
Kondo, Y.4
Yoshino, N.5
Abe, M.6
-
40
-
-
23944436906
-
Ferrocene-containing cationic lipids: Influence of redox state on cell transfection
-
DOI 10.1021/ja054038t
-
Abbott NL, Jewell CM, Hays ME, Kondo Y, Lynn DM. 2005. Ferrocene-containing cationic lipids: influence of redox state on cell transfection. J. Am. Chem. Soc. 127:11576-77 (Pubitemid 41208726)
-
(2005)
Journal of the American Chemical Society
, vol.127
, Issue.33
, pp. 11576-11577
-
-
Abbott, N.L.1
Jewell, C.M.2
Hays, M.E.3
Kondo, Y.4
Lynn, D.M.5
-
41
-
-
79958012417
-
Influence of biological media on the structure and behavior of ferrocene-Containing cationic lipid/DNA complexes used for DNA delivery
-
Golan S, Aytar BS, Muller JPE, Kondo Y, Lynn DM, et al. 2011. Influence of biological media on the structure and behavior of ferrocene-containing cationic lipid/DNA complexes used for DNA delivery. Langmuir 27:6615-21
-
(2011)
Langmuir.
, vol.27
, pp. 6615-6621
-
-
Golan, S.1
Aytar, B.S.2
Muller, J.P.E.3
Kondo, Y.4
Lynn, D.M.5
-
42
-
-
56749160538
-
Chemical activation of lipoplexes formed from DNA and a redox-active, ferrocene-Containing cationic lipid
-
Jewell CM, Hays ME, Kondo Y, Abbott NL, Lynn DM. 2008. Chemical activation of lipoplexes formed from DNA and a redox-active, ferrocene-containing cationic lipid. Bioconjug. Chem. 19:2120-28
-
(2008)
Bioconjug. Chem.
, vol.19
, pp. 2120-2128
-
-
Jewell, C.M.1
Hays, M.E.2
Kondo, Y.3
Abbott, N.L.4
Lynn, D.M.5
-
43
-
-
3343001331
-
Redox-active organometallic vesicles: Aqueous self-assembly of a diblock copolymer with a hydrophilic polyferrocenylsilane polyelectrolyte block
-
DOI 10.1002/anie.200352819
-
Power-Billard KN, Spontak RJ, Manners I. 2004. Redox-active organometallic vesicles: aqueous selfassembly of a diblock copolymer with a hydrophilic polyferrocenylsilane polyelectrolyte block. Angew. Chem. Int. Ed. Engl. 43:1260-64 (Pubitemid 39257947)
-
(2004)
Angewandte Chemie - International Edition
, vol.43
, Issue.10
, pp. 1260-1264
-
-
Power-Billard, K.N.1
Spontak, R.J.2
Manners, I.3
-
44
-
-
79958823872
-
Stimulus-Responsive self-Assembly: Reversible, redox-Controlled micellization of polyferrocenylsilane diblock copolymers
-
Eloi JC, Rider DA, Cambridge G, Whittell GR, Winnik MA, Manners I. 2011. Stimulus-responsive self-assembly: reversible, redox-controlled micellization of polyferrocenylsilane diblock copolymers. J. Am. Chem. Soc. 133:8903-13
-
(2011)
J. Am. Chem. Soc.
, vol.133
, pp. 8903-8913
-
-
Eloi, J.C.1
Rider, D.A.2
Cambridge, G.3
Whittell, G.R.4
Winnik, M.A.5
Manners, I.6
-
45
-
-
77955835980
-
Voltage-Responsive vesicles based on orthogonal assembly of two homopolymers
-
YanQA, Yuan JY, CaiZN, XinY,KangY,YinYW.2010. Voltage-responsive vesicles based on orthogonal assembly of two homopolymers. J. Am. Chem. Soc. 132:9268-70
-
(2010)
J. Am. Chem. Soc.
, vol.132
, pp. 9268-9270
-
-
Yan, Q.A.1
Yuan, J.Y.2
Cai, Z.N.3
Xin, Y.4
Kang, Y.5
Yin, Y.W.6
-
46
-
-
79953716819
-
Electrical switching between vesicles and micelles via redox-Responsive self-assembly of amphiphilic rod-coils
-
KimH, Jeong SM, Park JW.2011. Electrical switching between vesicles and micelles via redox-responsive self-assembly of amphiphilic rod-coils. J. Am. Chem. Soc. 133:5206-9
-
(2011)
J. Am. Chem. Soc.
, vol.133
, pp. 5206-5209
-
-
Kim, H.1
Jeong, S.M.2
Park, J.W.3
-
47
-
-
34347348305
-
PEG-SS-PPS: Reduction-sensitive disulfide block copolymer vesicles for intracellular drug delivery
-
DOI 10.1021/bm070085x
-
Cerritelli S, Velluto D, Hubbell JA. 2007. PEG-ss-PPS: reduction-sensitive disulfide block copolymer vesicles for intracellular drug delivery. Biomacromolecules 8:1966-72 (Pubitemid 47009977)
-
(2007)
Biomacromolecules
, vol.8
, Issue.6
, pp. 1966-1972
-
-
Cerritelli, S.1
Velluto, D.2
Hubbell, J.A.3
-
48
-
-
79960399848
-
Preparation and in vitro properties of redoxresponsive polymeric nanoparticles for paclitaxel delivery
-
Song N, Liu W, Tu Q, Liu R, Zhang Y, Wang J. 2011. Preparation and in vitro properties of redoxresponsive polymeric nanoparticles for paclitaxel delivery. Colloid Surf. B 87:454-63
-
(2011)
Colloid Surf.
, vol.B87
, pp. 454-463
-
-
Song, N.1
Liu, W.2
Tu, Q.3
Liu, R.4
Zhang, Y.5
Wang, J.6
-
49
-
-
0030591442
-
Liposomes with detachable polymer coating: Destabilization and fusion of dioleoylphosphatidylethanolamine vesicles triggered by cleavage of surface-grafted poly(ethylene glycol)
-
DOI 10.1016/0014-5793(96)00521-2
-
Kirpotin D, Hong KL, Mullah N, Papahadjopoulos D, Zalipsky S. 1996. Liposomes with detachable polymer coating: destabilization and fusion of dioleoylphosphatidylethanolamine vesicles triggered by cleavage of surface-grafted poly(ethylene glycol). FEBS Lett. 388:115-18 (Pubitemid 26226342)
-
(1996)
FEBS Letters
, vol.388
, Issue.2-3
, pp. 115-118
-
-
Kirpotin, D.1
Hong, K.2
Mullah, N.3
Papahadjopoulos, D.4
Zalipsky, S.5
-
50
-
-
0035575844
-
Targeted delivery and triggered release of liposomal doxorubicin enhances cytotoxicity against human B lymphoma cells
-
DOI 10.1016/S0005-2736(01)00409-6, PII S0005273601004096
-
Ishida T, Kirchmeier MJ, Moasea EH, Zalipsky S, Allena TM. 2001. Targeted delivery and triggered release of liposomal doxorubicin enhances cytotoxicity against human B lymphoma cells. Biochim. Biophys. Acta 1515:144-58 (Pubitemid 33086831)
-
(2001)
Biochimica et Biophysica Acta - Biomembranes
, vol.1515
, Issue.2
, pp. 144-158
-
-
Ishida, T.1
Kirchmeier, M.J.2
Moase, E.H.3
Zalipsky, S.4
Allen, T.M.5
-
51
-
-
0033199557
-
New detachable poly(ethylene glycol) conjugates: Cysteine-cleavable lipopolymers regenerating natural phospholipid, diacyl phosphatidylethanolamine
-
DOI 10.1021/bc990031n
-
Zalipsky S, QazenM,Walker JA, Mullah N, Quinn YP, Huang SK. 1999. New detachable poly(ethylene glycol) conjugates: cysteine-cleavable lipopolymers regenerating natural phospholipid, diacyl phosphatidylethanolamine. Bioconjug. Chem. 10:703-7 (Pubitemid 29456355)
-
(1999)
Bioconjugate Chemistry
, vol.10
, Issue.5
, pp. 703-707
-
-
Zalipsky, S.1
Qazen, M.2
Walker II, J.A.3
Mullah, N.4
Quinn, Y.P.5
Huang, S.K.6
-
52
-
-
0025088074
-
Development of a drug-release strategy based on the reductive fragmentation of benzyl carbamate disulfides
-
DOI 10.1021/jo00296a082
-
Senter PD, Pearce WE, Greenfield RS. 1990. Development of a drug-release strategy based on the reductive fragmentation of benzyl carbamate disulfides. J. Org. Chem. 55:2975-78 (Pubitemid 20296593)
-
(1990)
Journal of Organic Chemistry
, vol.55
, Issue.9
, pp. 2975-2978
-
-
Senter, P.D.1
Pearce, W.E.2
Greenfield, R.S.3
-
54
-
-
0014139748
-
The standard redox potential of cysteine-cystine from the thiol-disulphide exchange reaction with glutathione and lipoic acid
-
Jocelyn PC. 1967. The standard redox potential of cysteine-cystine from the thiol-disulphide exchange reaction with glutathione and lipoic acid. Eur. J. Biochem. 2:327-31
-
(1967)
Eur. J. Biochem.
, vol.2
, pp. 327-331
-
-
Jocelyn, P.C.1
-
55
-
-
80052219412
-
Reduction-Sensitive liposomes from amultifunctional lipid conjugate and natural phospholipids: Reduction and release kinetics and cellular uptake
-
Goldenbogen BR, Brodersen N, Gramatica A, Loew M, Liebscher JR, et al. 2011. Reduction-sensitive liposomes from amultifunctional lipid conjugate and natural phospholipids: reduction and release kinetics and cellular uptake. Langmuir 27:10820-29
-
(2011)
Langmuir.
, vol.27
, pp. 10820-29
-
-
Goldenbogen, B.R.1
Brodersen, N.2
Gramatica, A.3
Loew, M.4
Liebscher, J.R.5
-
57
-
-
0015526371
-
Stereopopulation control i rate enhancement in lactonizations of orthohydroxyhydrocinnamic acids
-
Milstien S, Cohen LA. 1972. Stereopopulation control. I. Rate enhancement in lactonizations of orthohydroxyhydrocinnamic acids. J. Am. Chem. Soc. 94:9158-65
-
(1972)
J. Am. Chem. Soc.
, Issue.94
, pp. 9158-9165
-
-
Milstien, S.1
Cohen, L.A.2
-
58
-
-
0001464558
-
Reductive lactonization of strategically methylated quinone propionic-acid esters and amides
-
Carpino LA, Triolo SA, Berglund RA. 1989. Reductive lactonization of strategically methylated quinone propionic-acid esters and amides. J. Org. Chem. 54:3303-10
-
(1989)
J. Org. Chem.
, vol.54
, pp. 3303-3310
-
-
Carpino, L.A.1
Triolo, S.A.2
Berglund, R.A.3
-
59
-
-
0001654224
-
Development of a novel redox-Sensitive protecting group for amines which utilizes a facilitated lactonization reaction
-
Wang BH, Liu SM, Borchardt RT. 1995. Development of a novel redox-sensitive protecting group for amines which utilizes a facilitated lactonization reaction. J. Org. Chem. 60:539-43
-
(1995)
J. Org. Chem.
, vol.60
, pp. 539-543
-
-
Wang, B.H.1
Liu, S.M.2
Borchardt, R.T.3
-
60
-
-
37549039125
-
Chemical synthesis and biological evaluation of a NAD(P)H:quinone oxidoreductase 1-Targeted tripartite quinone drug delivery system
-
Volpato M, Abou-Zeid N, Tanner RW, Glassbrook LT, Taylor J, et al. 2007. Chemical synthesis and biological evaluation of a NAD(P)H:quinone oxidoreductase 1-targeted tripartite quinone drug delivery system. Mol. Cancer Ther. 6:3122-30
-
(2007)
Mol. Cancer Ther.
, vol.6
, pp. 3122-3130
-
-
Volpato, M.1
Abou-Zeid, N.2
Tanner, R.W.3
Glassbrook, L.T.4
Taylor, J.5
-
61
-
-
0034541288
-
Reductive and bioreductive activation is controlled by electronic properties of substituents in conformationally-constrained anticancer drug delivery systems
-
Weerapreeyakul N, Visser P, BrummelhuisM, Gharat L, Chikhale PJ. 2000. Reductive and bioreductive activation is controlled by electronic properties of substituents in conformationally constrained anticancer drug delivery systems. Med. Chem. Res. 10:149-63 (Pubitemid 32014482)
-
(2000)
Medicinal Chemistry Research
, vol.10
, Issue.3
, pp. 149-163
-
-
Weerapreeyakul, N.1
Visser, P.2
Brummelhuis, M.3
Gharat, L.4
Chikhale, P.J.5
-
62
-
-
0017886452
-
2 from equilibrium reactions with flavodoxins, methyl viologen and hydrogen plus hydrogenase
-
DOI 10.1111/j.1432-1033.1978.tb12269.x
-
Mayhew SG. 1978. The redox potential of dithionite and SO2 - from equilibrium reactions with flavodoxins, methyl viologen and hydrogen plus hydrogenase. Eur. J. Biochem. 5:535-47 (Pubitemid 8335277)
-
(1978)
European Journal of Biochemistry
, vol.85
, Issue.2
, pp. 535-547
-
-
Mayhew, S.G.1
-
63
-
-
0343657559
-
Concurrent general-Acid and general-Base catalysis of esterification
-
Milstien S, Cohen LA. 1970. Concurrent general-acid and general-base catalysis of esterification. J. Am. Chem. Soc. 92:4377-82
-
(1970)
J. Am. Chem. Soc.
, vol.92
, pp. 4377-4382
-
-
Milstien, S.1
Cohen, L.A.2
-
65
-
-
0040401549
-
Theory of stationary electrode polarography-Single scan and cyclic methods applied to reversible irreversible and kinetic systems
-
NicholsonRS, Shain I. 1964. Theory of stationary electrode polarography-single scan and cyclic methods applied to reversible irreversible and kinetic systems. Anal. Chem. 36:706-23
-
(1964)
Anal. Chem.
, vol.36
, pp. 706-723
-
-
Nicholson, R.S.1
Shain, I.2
-
66
-
-
0001377673
-
Mechanism of the oxidation of NADH by quinones-Energetics of oneelectron and hydride routes
-
Carlson BW, Miller LL. 1985. Mechanism of the oxidation of NADH by quinones-energetics of oneelectron and hydride routes. J. Am. Chem. Soc. 107:479-85
-
(1985)
J. Am. Chem. Soc.
, vol.107
, pp. 479-485
-
-
Carlson, B.W.1
Miller, L.L.2
-
67
-
-
80053530237
-
Shedding light by cancer redox-human NAD(P)H: Quinone oxidoreductase 1 activation of a cloaked fluorescent dye
-
SilversWC, Payne AS, McCarley RL. 2011. Shedding light by cancer redox-human NAD(P)H: quinone oxidoreductase 1 activation of a cloaked fluorescent dye. Chem. Commun. 47:11264-66 www.
-
(2011)
Chem. Commun.
, vol.47
, pp. 11264-11266
-
-
Silvers, W.C.1
Payne, A.S.2
McCarley, R.L.3
|