[1] Cruz-Cabeza A J, Reutzel-Edens S M, Bernstein J. Facts and fictions about polymorphism[J]. Chemical Society Reviews,2015, 44(23):8619-8635
[2] Hilfiker, R. Polymorphism in the pharmaceutical industry[M]. Weinheim, Germany:Wiley-VCH, 2006
[3] Karthika S, Radhakrishnan T K, Kalaichelvi P. A review of classical and nonclassical nucleation theories[J]. Crystal Growth & Design,2016, 16(11):6663-6681
[4] Erdemir D, Lee A Y, Myerson A S. Nucleation of crystals from solution:Classical and two-step models[J]. Accounts of Chemical Research,2009, 42(5):621-629
[5] Davey R J, Schroeder S L M, Ter Horst J H, et al. Nucleation of organic crystals-A molecular perspective[J]. Angewandte Chemie International Edition, 2013, 52(8):2166-2179
[6] Cavallo D, Alfonso G C. Concomitant crystallization and cross-nucleation in polymorphic polymers[M]. Germany:Springer International Publishing, 2017
[7] Desgranges C, Delhommelle J. Molecular mechanism for the cross-nucleation between polymorphs[J]. Journal of the American Chemical Society,2006, 128(32):10368-10369
[8] Yu L. Nucleation of one polymorph by another[J]. Journal of the American Chemical Society,2003, 125(21):6380-6381
[9] Bernstein J, Davey R J, Henck J O. Concomitant polymorphs[J]. Angewandte Chemie International Edition,1999, 38(23):3440-3461
[10] 杜威. 普拉格雷盐酸盐伴随多晶型和托芬那酸构象多晶型行为研究[D]. 天津:天津大学, 2015 Du Wei. A study on concomitant polymorphism of prasugrel hydrochloride and conformational polymorphism of tolfenamic acid[D]. Tianjin:Tianjin University, 2015(in Chinese)
[11] Du W, Yin Q, Bao Y, et al. Concomitant polymorphism of prasugrel hydrochloride in reactive crystallization[J]. Industrial & Engineering Chemistry Research,2013, 52(46):16182-16189
[12] Jiang S, Horst J H T, Jansens P J. Concomitant polymorphism of o-aminobenzoic acid in antisolvent crystallization[J]. Crystal Growth & Design,2008, 8(1):37-43
[13] Kitamura M. Strategy for control of crystallization of polymorphs[J]. Cryst Eng Comm,2009, 11(6):949-964
[14] Llinàs A, Goodman J M. Polymorph control:Past, present and future[J]. Drug Discovery Today,2008, 13(5):198-210
[15] Newman A. Specialized solid form screening techniques[J]. Organic Process Research & Development, 2013, 17(3):457-471
[16] Gu C, Li H, Gandhi R B, et al. Grouping solvents by statistical analysis of solvent property parameters:Implication to polymorph screening[J]. International Journal of Pharmaceutics,2004, 283(1):117-125
[17] Zeglinski J, Kuhs M, Khamar D, et al. Crystal nucleation of tolbutamide in solution:Relationship to solvent, solute conformation, and solution structure[J]. Chemistry-A European Journal,2018, 24(19):4916-4926
[18] Beckmann W. Seeding the desired polymorph:Background, possibilities, limitations, and case studies[J]. Org process Res Dev,2000, 4(5):372-383
[19] Mo Y, Dang L, Wei H. L-Glutamic acid polymorph control using amino acid additives[J]. Industrial & Engineering Chemistry Research,2011, 50(18):10385-10392
[20] Simone E, Steele G, Nagy Z K. Tailoring crystal shape and polymorphism using combinations of solvents and a structurally related additive[J]. Cryst Eng Comm,2015, 17(48):9370-9379
[21] Weissbuch I, Leisorowitz L, Lahav M."Tailor-Made"and charge-transfer auxiliaries for the control of the crystal polymorphism of glycine[J]. Advanced Materials, 1994, 6(12):952-956
[22] Dowling R, Davey R J, Curtis R A, et al. Acceleration of crystal growth rates:An unexpected effect of tailor-made additives[J]. Chemical Communications,2010, 46(32):5924-5926
[23] Gu C, Chatterjee K, Young V, et al. Stabilization of a metastable polymorph of sulfamerazine by structurally related additives[J]. Journal of Crystal Growth, 2002, 235(1):471-481
[24] Ventura S P M, E Silva F A, Quental M V, et al. Ionic-Liquid-Mediated extraction and separation processes for bioactive compounds:Past, present, and future trends[J]. Chemical Reviews,2017, 117(10):6984-7052
[25] An J, Jin F, Kim H S, et al. Application of ionic liquid to polymorphic transformation of anti-viral/HIV drug adefovir dipivoxil[J]. Archives of Pharmacal Research, 2016, 39(5):646-659
[26] Martins I C B, Gomes J R B, Duarte M T, et al. Understanding polymorphic control of pharmaceuticals using imidazolium-based ionic liquid mixtures as crystallization directing agents[J]. Crystal Growth & Design, 2017, 17(2):428-432
[27] An J H, Kim J M, Chang S M, et al. Application of ionic liquid to polymorphic design of pharmaceutical ingredients[J]. Crystal Growth & Design, 2010, 10(7):3044-3050
[28] An J H, Kim W S. Antisolvent crystallization using ionic liquids as solvent and antisolvent for polymorphic design of active pharmaceutical ingredient[J]. Crystal Growth & Design, 2013, 13(1):31-39
[29] An J H, Jin F, Kim H S, et al. Investigation of the polymorphic transformation of the active pharmaceutical ingredient clopidogrel bisulphate using the ionic liquid AEImBF4[J]. Crystal Growth & Design,2016, 16(4)
[30] Zeng Q, Mukherjee A, Müller P, et al. Exploring the role of ionic liquids to tune the polymorphic outcome of organic compounds[J]. Chemical Science,2017, 9(6)
[31] Lang M, Grzesiak A L, Matzger A J. The use of polymer heteronuclei for crystalline polymorph selection[J]. Journal of the American Chemical Society, 2002, 124(50):14834-14835
[32] Price C P, Grzesiak A L, Matzger A J. Crystalline polymorph selection and discovery with polymer heteronuclei[J]. Journal of the American Chemical Society, 2005, 127(15):5512-5517
[33] Foroughi L M, Kang Y N, Matzger A J. Polymer-Induced heteronucleation for protein single crystal growth:Structural elucidation of bovine liver catalase and concanavalin A forms[J]. Crystal Growth & Design, 2011, 11(4):1294-1298
[34] López-Mejías V, Knight J L, Brooks C L, et al. On the mechanism of crystalline polymorph selection by polymer heteronuclei[J]. Langmuir, 2011, 27(12):7575-7579
[35] Pfund L Y, Price C P, Frick J J, et al. Controlling pharmaceutical crystallization with designed polymeric heteronuclei[J]. Journal of the American Chemical Society,2015, 137(2):871-875
[36] Frank D S, Matzger A J. Influence of chemical functionality on the rate of polymer-induced heteronucleation[J]. Crystal Growth & Design, 2017, 17(8):4056-4059
[37] Quiñones R, Brown R T, Searls N, et al. Study of polymorphism using patterned self-assembled monolayers approach on metal substrates[J]. Applied Surface Science,2018, 427:97-105
[38] Harano K, Homma T, Niimi Y, et al. Heterogeneous nucleation of organic crystals mediated by single-molecule templates[J]. Nature Materials,2012, 11(10):877-881
[39] Hiremath R, Basile J A, And S W V, et al. Controlling molecular crystal polymorphism with self-assembled monolayer templates[J]. Journal of the American Chemical Society,2005, 127(51):18321-18327
[40] Cui Y, Stojakovic J, Kijima H, et al. Mechanism of contact-induced heterogeneous nucleation[J]. Crystal Growth & Design, 2016, 16(10):6131-6138
[41] Zhang J, Liu A, Han Y, et al. Effects of self-assembled monolayers on selective crystallization of tolbutamide[J]. Crystal Growth & Design,2011, 11(11):5498-5506
[42] Yang X, Sarma B, Myerson A S. Polymorph control of micro/nano-sized mefenamic acid crystals on patterned self-assembled monolayer islands[J]. Crystal Growth & Design,2012, 12(12):5521-5528
[43] Shi H, Xiao Y, Ferguson S, et al. Progress of crystallization in microfluidic devices[J]. Lab on a Chip, 2017, 17(13):2167-2185
[44] 蒋楠. 液滴-微流体环境下L-谷氨酸多晶型现象研究[D]. 天津:天津大学, 2016 Jiang Nan. The polymorph studies of L-glutanmic acid under droplet-microfluidic system[D]. Tianjin:Tianjin University, 2016(in Chinese)
[45] And O G, Peter G V. Are nucleation kinetics of protein crystals similar to those of liquid droplets?[J]. J Am Chem Soc, 2000, 122(1):156-163
[46] Yamaguchi H, Maeki M, Yamashita K, et al. Controlling one protein crystal growth by droplet-based microfluidic system[J]. Journal of Biochemistry, 2013, 153(4):339-346
[47] Maeki M, Yoshizuka S, Yamaguchi H, et al. X-Ray diffraction of protein crystal grown in a nano-liter scale droplet in a microchannel and evaluation of its applicability[J]. Analytical Sciences, 2012, 28(28):65
[48] Laval P, Giroux C, Leng J, et al. Microfluidic screening of potassium nitrate polymorphism[J]. Journal of Crystal Growth, 2008, 310(12):3121-3124
[49] Ding L, Zong S, Dang L, et al. Effects of inorganic additives on polymorphs of glycine in microdroplets[J]. Cryst Eng Comm,2017, 20(2)
[50] Jiang N, Wang Z, Dang L, et al. Effect of supersaturation on L-glutamic acid polymorphs under droplet-based microchannels[J]. Journal of Crystal Growth,2016, 446:68-73
[51] Teshima Y, Maeki M, Yamashita K, et al. A method for generating a metastable crystal in a microdroplet[J]. Crystengcomm,2013, 15(46):9874-9877
[52] Chemburkar S R, Bauer J, Deming K, et al. Dealing with the impact of ritonavir polymorphs on the late stages of bulk drug process development[J]. Organic Process Research & Development,2000, 4(5):413-417
[53] Du W, Yin Q, Hao H. Solution-Mediated polymorphic transformation of prasugrel hydrochloride from form Ⅱ to Form I[J]. Industrial & Engineering Chemistry Research, 2014, 53(14):5652-5659
[54] Jiang S, Jansens P J, ter Horst J H. Mechanism and kinetics of the polymorphic transformation of o-aminobenzoic acid[J]. Crystal Growth & Design, 2010, 10(5):2123-2128
[55] Wu C D, Lin W. Highly Porous, Homochiral metal-organic frameworks:Solvent-exchange-induced single-crystal to single-crystal transformations[J]. Angewandte Chemie International Edition,2005, 44(13):1958-1961
[56] 龚俊波,王琦,董伟兵,等. 药物晶型转化与控制的研究进展[J]. 化工学报, 2013, (2):385-392 Gong Junbo, Wang Qi, Dong Weibing, et al. Progress on transformation and manipulation of drug polymorphism[J]. Journal of Chemical Industry and Engineering, 2013, (2):385-392(in Chinese)
[57] Mangin D, Puel F, Veesler S. Polymorphism in processes of crystallization in solution:A practical review[J]. Organic Process Research & Development, 2009, 13(6):1241-1253
[58] Wu S, Shen H, Li K, et al. Agglomeration mechanism of azithromycin dihydrate in acetone-water mixtures and optimization of the powder properties[J]. Industrial & Engineering Chemistry Research, 2016, 55(17):4905-4910
[59] Wu S, Du Shichao, Chen M, et al. Crystal structures and phase behavior of sulfadiazine and a method for the preparation of aggregates with good performance[J]. Chemical Engineering & Technology, 2018, 41(3):532-540
[60] Wu S, Chen M, Li K, et al. Solvent penetration mediated phase transformation for the preparation of aggregated particles with well-defined shape[J]. Cryst Eng Comm. 2016, 18(48):9223-9226
|