Kabanov A V, Batrakova E V, Alakhov V Y. Pluronic(R) block copolymers as novel polymer therapeutics for drug and gene delivery [J]. Journal of Controlled Release, 2002, 82(2/3): 189-212.
[2]
Kabanov A V, Lemieux P, Vinogradov S, et al. Pluronic(R) block copolymers: novel functional molecules for gene therapy [J]. Advanced Drug Delivery Reviews, 2002, 54(2): 223-233.
[3]
Verger R.“Interfacial activation” of lipases: facts and artifacts [J]. Trends in Biotechnology, 1997, 15(1): 32-38.
[4]
Laane C, Boeren S, Vos K, et al. Rules for optimization of biocatalysis in organic solvents [J]. Biotechnology and Bioengineering, 1987, 30(1): 81-87.
[5]
Cambou B, Klibanov A M. Preparative production of optically-active esters and alcohols using esterase-catalyzed stereospecific trans-esterification in organic media [J]. Journal of the American Chemical Society, 1984, 106(9): 2687-2692.
[6]
Zaks A, Klibanov A M. Enzymatic catalysis in organic media at 100-degrees-C [J]. Science, 1984, 224(4654): 1249-1251.
[7]
Gross R A, Ganesh M, Lu W. Enzyme-catalysis breathes new life into polyester condensation polymerizations [J]. Trends in Biotechnology, 2010, 28(8): 435-443.
[8]
Wangikar P P, Michels P C, Clark D S, et al. Structure and function of subtilisin BPN'solubilized in organic solvents [J]. Journal of the American Chemical Society, 1997, 119(1): 70-76.
[9]
Klibanov A M. Why are enzymes less active in organic solvents than in water? [J]. Trends in Biotechnology, 1997, 15(3): 97-101.
[10]
Zaks A, Klibanov A M. The effect of water on enzyme action in organic media [J]. Journal of Biological Chemistry, 1988, 263(17): 8017-8021.
[11]
Ge J, Yang C, Zhu J, et al. Nanobiocatalysis in organic media: opportunities for enzymes in nanostructures [J]. Topics in Catalysis, 2012, 55(16/17/18): 1070-1080.
[12]
Carrea G, Riva S. Properties and synthetic applications of enzymes in organic solvents [J]. Angewandte Chemie-International Edition, 2000, 39(13): 2226-2254.
[13]
Almarsson O, Klibanov A M. Remarkable activation of enzymes in nonaqueous media by denaturing organic cosolvents [J]. Biotechnology and Bioengineering, 1996, 49(1): 87-92.
[14]
Kim J, Grate J W. Single-enzyme nanoparticles armored by a nanometer-scale organic/inorganic network [J]. Nano Letters, 2003, 3(9): 1219-1222.
[15]
Ge J, Lu D, Wang J, et al. Lipase nanogel catalyzed transesterification in anhydrous dimethyl sulfoxide [J]. Biomacromolecules, 2009, 10(6): 1612-1618.
[16]
Ge J, Lei J, Zare R N. Protein-inorganic hybrid nanoflowers [J]. Nature Nanotechnology, 2012, 7(7): 428-432.
[17]
Nardin C, Thoeni S, Widmer J, et al. Nanoreactors based on (polymerized) ABA-triblock copolymer vesicles [J]. Chem. Commun., 2000, (15): 1433-1434.
[18]
Grotzky A, Nauser T, Erdogan H, et al. A fluorescently labeled dendronized polymer–enzyme conjugate carrying multiple copies of two different types of active enzymes [J]. Journal of the American Chemical Society, 2012, 134(28): 11392-11395.
[19]
Zhu J, Zhang Y, Lu D, Zare R N, Ge J, Liu Z. Temperature-responsive enzyme-polymer nanoconjugates with enhanced catalytic activities in organic media [J]. Chemical Communications, 2013, 49: 6090-6092.
[20]
Zhang Y, Dai Y, Hou M, et al. Chemo-enzymatic synthesis of valrubicin using Pluronic conjugated lipase with temperature responsiveness in organic media [J]. RSC Advances, 2013, 3(45): 22963-22966.
[21]
Chang E, Galvez M G, Glotzbach J P, et al. Vascular anastomosis using controlled phase transitions in poloxamer gels [J]. Nature Medicine, 2011, 17(9): 1147-1152.
