A mini review on the functional biomaterials based on poly (lactic acid) stereocomplex

Nanocarriers as an emerging platform for cancer therapy

Peer, D., Karp, J. M., Hong, S., Farokhzad, O. C., Margalit, R., & Langer, R. (2007) · Nature Nanotechnology · doi:10.1038/nnano.2007.387 · Cited by 8,710 · see citing works

Hydrogels for Tissue Engineering

Lee, K. Y., & Mooney, D. J. (2001) · Chemical Reviews · doi:10.1021/cr000108x · Cited by 5,295 · see citing works

Synthetic biomaterials as instructive extracellular microenvironments for morphogenesis in tissue engineering

Lutolf, M. P., & Hubbell, J. A. (2005) · Nature Biotechnology · doi:10.1038/nbt1055 · Cited by 4,551 · see citing works

Physical hydrogels composed of polyampholytes demonstrate high toughness and viscoelasticity

Sun, T. L., Kurokawa, T., Kuroda, S., Ihsan, A. B., Akasaki, T., Sato, K., Haque, M. A., Nakajima, T., & Gong, J. P. (2013) · Nature Materials · doi:10.1038/nmat3713 · Cited by 2,089 · see citing works

Biodegradable block copolymers as injectable drug-delivery systems

Jeong, B., Bae, Y. H., Lee, D. S., & Kim, S. W. (1997) · Nature · doi:10.1038/42218 · Cited by 1,999 · see citing works

Novel crosslinking methods to design hydrogels

Hennink, W. E., & van Nostrum, C. F. (2002) · Advanced Drug Delivery Reviews · doi:10.1016/s0169-409x(01)00240-x · Cited by 1,979 · see citing works

Photodegradable Hydrogels for Dynamic Tuning of Physical and Chemical Properties

Kloxin, A. M., Kasko, A. M., Salinas, C. N., & Anseth, K. S. (2009) · Science · doi:10.1126/science.1169494 · Cited by 1,748 · see citing works

Photopolymerizable hydrogels for tissue engineering applications

Nguyen, K. T., & West, J. L. (2002) · Biomaterials · doi:10.1016/s0142-9612(02)00175-8 · Cited by 1,669 · see citing works

Block copolymer micelles: preparation, characterization and application in drug delivery

Gaucher, G., Dufresne, M.-H., Sant, V. P., Kang, N., Maysinger, D., & Leroux, J.-C. (2005) · Journal of Controlled Release · doi:10.1016/j.jconrel.2005.09.034 · Cited by 1,498 · see citing works

Injectable and biodegradable hydrogels: gelation, biodegradation and biomedical applications

Li, Y., Rodrigues, J., & Tomás, H. (2011) · Chemical Society Reviews · doi:10.1039/c1cs15203c · Cited by 1,451 · see citing works

Stereocomplex formation between enantiomeric poly(lactides)

Ikada, Y., Jamshidi, K., Tsuji, H., & Hyon, S. H. (1987) · Macromolecules · doi:10.1021/ma00170a034 · Cited by 1,409 · see citing works

Poly(lactide) Stereocomplexes: Formation, Structure, Properties, Degradation, and Applications

Tsuji, H. (2005) · Macromolecular Bioscience · doi:10.1002/mabi.200500062 · Cited by 1,366 · see citing works

Polymeric micelles—A new generation of colloidal drug carriers

Jones, M.-C., & Leroux, J.-C. (1999) · European Journal of Pharmaceutics and Biopharmaceutics · doi:10.1016/s0939-6411(99)00039-9 · Cited by 1,256 · see citing works

Stereocomplex Formation between Enantiomeric Poly(lactide)s

박은하, & 진인주 (2010) · 한국고분자학회 학술대회 연구논문 초록집 · Cited by 1,084 · see citing works

Poly(lactide) Stereocomplexes: Formation, Structure, Properties, Degradation, and Applications

Tsuji, H. (2007) · Macromolecular Bioscience · doi:10.1002/mabi.200700275 · Cited by 1,021 · see citing works

Photoencapsulation of osteoblasts in injectable RGD-modified PEG hydrogels for bone tissue engineering

Burdick, J. A., & Anseth, K. S. (2002) · Biomaterials · doi:10.1016/s0142-9612(02)00176-x · Cited by 1,008 · see citing works

Cross-linked block copolymer micelles: functional nanostructures of great potential and versatility

O’Reilly, R. K., Hawker, C. J., & Wooley, K. L. (2006) · Chemical Society Reviews · doi:10.1039/b514858h · Cited by 939 · see citing works

In situ gelling stimuli-sensitive block copolymer hydrogels for drug delivery

He, C., Kim, S. W., & Lee, D. S. (2008) · Journal of Controlled Release · doi:10.1016/j.jconrel.2008.01.005 · Cited by 870 · see citing works

Small functional groups for controlled differentiation of hydrogel-encapsulated human mesenchymal stem cells

Benoit, D. S. W., Schwartz, M. P., Durney, A. R., & Anseth, K. S. (2008) · Nature Materials · doi:10.1038/nmat2269 · Cited by 825 · see citing works

Micellar carriers based on block copolymers of poly(ε-caprolactone) and poly(ethylene glycol) for doxorubicin delivery

Shuai, X., Ai, H., Nasongkla, N., Kim, S., & Gao, J. (2004) · Journal of Controlled Release · doi:10.1016/j.jconrel.2004.06.003 · Cited by 695 · see citing works

In situ gelling hydrogels for pharmaceutical and biomedical applications

Tomme, S. R. V., Storm, G., & Hennink, W. E. (2008) · International Journal of Pharmaceutics · doi:10.1016/j.ijpharm.2008.01.057 · Cited by 625 · see citing works

Thermoreversible Gelation of PEG−PLGA−PEG Triblock Copolymer Aqueous Solutions

Jeong, B., Bae, Y. H., & Kim, S. W. (1999) · Macromolecules · doi:10.1021/ma9908999 · Cited by 618 · see citing works

Disulfide Cross-Linked Hyaluronan Hydrogels

Shu, X. Z., Liu, Y., Luo, Y., et al. (2002) · Biomacromolecules · doi:10.1021/bm025603c · Cited by 618 · see citing works

Mechanism of the Stereocomplex Formation between Enantiomeric Poly(lactide)s

Brizzolara, D., Cantow, H.-J., Diederichs, K., Keller, E., & Domb, A. J. (1996) · Macromolecules · doi:10.1021/ma951144e · Cited by 547 · see citing works

Stereocomplex formation between enantiomeric poly(lactic acid)s. XI. Mechanical properties and morphology of solution-cast films

Tsuji, H., & Ikada, Y. (1999) · Polymer · doi:10.1016/s0032-3861(99)00004-x · Cited by 545 · see citing works

Crystallization behaviour of poly(l-lactide)

Miyata, T., & Masuko, T. (1998) · Polymer · doi:10.1016/s0032-3861(97)10203-8 · Cited by 498 · see citing works

Hierarchically biomimetic bone scaffold materials: nano‐HA/collagen/PLA composite

Liao, S. S., Cui, F. Z., Zhang, W., & Feng, Q. L. (2004) · Journal of Biomedical Materials Research Part B: Applied Biomaterials · doi:10.1002/jbm.b.20035 · Cited by 487 · see citing works

Nanoparticles as contrast agents for in-vivo bioimaging: current status and future perspectives

Hahn, M. A., Singh, A. K., Sharma, P., Brown, S. C., & Moudgil, B. M. (2010) · Analytical and Bioanalytical Chemistry · doi:10.1007/s00216-010-4207-5 · Cited by 484 · see citing works

Injectable and bioresponsive hydrogels for on-demand matrix metalloproteinase inhibition

Purcell, B. P., Lobb, D. C., Charati, M. B., Dorsey, S. M., Wade, R. J., Zellars, K. N., Doviak, H., Pettaway, S., Logdon, C. B., Shuman, J. A., et al. (2014) · Nature Materials · doi:10.1038/nmat3922 · Cited by 480 · see citing works

Methoxy poly(ethylene glycol)-poly(lactide) (MPEG-PLA) nanoparticles for controlled delivery of anticancer drugs

Dong, Y., & Feng, S. (2003) · Biomaterials · doi:10.1016/j.biomaterials.2003.09.055 · Cited by 468 · see citing works

Self-assembly of short peptides to form hydrogels: Design of building blocks, physical properties and technological applications

Fichman, G., & Gazit, E. (2013) · Acta Biomaterialia · doi:10.1016/j.actbio.2013.08.013 · Cited by 463 · see citing works

Stereocomplexed polylactides (Neo‐PLA) as high‐performance bio‐based polymers: their formation, properties, and application

Fukushima, K., & Kimura, Y. (2006) · Polymer International · doi:10.1002/pi.2010 · Cited by 435 · see citing works

Polylactide stereochemistry: effect on enzymic degradability

Reeve, M. S., McCarthy, S. P., Downey, M. J., & Gross, R. A. (1994) · Macromolecules · doi:10.1021/ma00081a030 · Cited by 433 · see citing works

Stereocomplex formation between enantiomeric poly(lactic acids). 9. Stereocomplexation from the melt

Tsuji, H., & Ikada, Y. (1993) · Macromolecules · doi:10.1021/ma00077a032 · Cited by 410 · see citing works

Infrared Spectroscopic Study of CH3···OC Interaction during Poly( l -lactide)/Poly( d -lactide) Stereocomplex Formation

Zhang, J., Sato, H., Tsuji, H., Noda, I., & Ozaki, Y. (2005) · Macromolecules · doi:10.1021/ma047872w · Cited by 395 · see citing works

Crystal structure of stereocomplex of poly(L-lactide) and poly(D-lactide)

Okihara, T., Tsuji, M., Kawaguchi, A., Katayama, K.-I., Tsuji, H., Hyon, S.-H., & Ikada, Y. (1991) · Journal of Macromolecular Science Part B · doi:10.1080/00222349108245788 · Cited by 382 · see citing works

Isothermal and non-isothermal crystallization behavior of poly(l-lactic acid): Effects of stereocomplex as nucleating agent

Tsuji, H., Takai, H., & Saha, S. K. (2006) · Polymer · doi:10.1016/j.polymer.2006.03.074 · Cited by 353 · see citing works

Biodegradable and thermoreversible PCLA–PEG–PCLA hydrogel as a barrier for prevention of post-operative adhesion

Zhang, Z., Ni, J., Chen, L., Yu, L., Xu, J.-W., & Ding, J. (2011) · Biomaterials · doi:10.1016/j.biomaterials.2011.03.046 · Cited by 339 · see citing works

Shear‐Thinning Supramolecular Hydrogels with Secondary Autonomous Covalent Crosslinking to Modulate Viscoelastic Properties In Vivo

Rodell, C. B., MacArthur, J. W., Dorsey, S. M., Wade, R. J., Wang, L. L., Woo, Y.-P. J., & Burdick, J. A. (2014) · Advanced Functional Materials · doi:10.1002/adfm.201403550 · Cited by 338 · see citing works

Stereocomplex Block Copolymer Micelles: Core−Shell Nanostructures with Enhanced Stability

Kang, N., Perron, M., Prud'homme, R. E., Zhang, Y., Gaucher, G., & Leroux, J. (2005) · Nano Letters · doi:10.1021/nl048037v · Cited by 334 · see citing works

An injectable calcium phosphate-alginate hydrogel-umbilical cord mesenchymal stem cell paste for bone tissue engineering

Zhao, L., Weir, M. D., & Xu, H. H. K. (2010) · Biomaterials · doi:10.1016/j.biomaterials.2010.05.017 · Cited by 334 · see citing works

Stereocomplex formation between enantiomeric poly(lactic acid)s. 3. Calorimetric studies on blend films cast from dilute solution

Tsuji, H., Hyon, S. H., & Ikada, Y. (1991) · Macromolecules · doi:10.1021/ma00020a026 · Cited by 334 · see citing works

Injectable Biomaterials for Regenerating Complex Craniofacial Tissues

Kretlow, J. D., Young, S. W., Klouda, L., Wong, M. E., & Mikos, A. G. (2009) · Advanced Materials · doi:10.1002/adma.200802009 · Cited by 302 · see citing works

Polylactide (PLA)-based amphiphilic block copolymers: synthesis, self-assembly, and biomedical applications

Oh, J. K. (2011) · Soft Matter · doi:10.1039/c0sm01539c · Cited by 302 · see citing works

Enhanced thermal stability of poly(lactide)s in the melt by enantiomeric polymer blending

Tsuji, H., & Fukui, I. (2003) · Polymer · doi:10.1016/s0032-3861(03)00175-7 · Cited by 275 · see citing works

Melt preparation and nucleation efficiency of polylactide stereocomplex crystallites

Anderson, K. S., & Hillmyer, M. A. (2006) · Polymer · doi:10.1016/j.polymer.2006.01.062 · Cited by 254 · see citing works

Investigation of Phase Transitional Behavior of Poly( l -lactide)/Poly( d -lactide) Blend Used to Prepare the Highly-Oriented Stereocomplex

Zhang, J., Tashiro, K., Tsuji, H., & Domb, A. J. (2007) · Macromolecules · doi:10.1021/ma061693s · Cited by 237 · see citing works

Stereocomplex formation between enantiomeric poly(lactic acid)s. 2. Stereocomplex formation in concentrated solutions

Tsuji, H., Horii, F., Hyon, S. H., & Ikada, Y. (1991) · Macromolecules · doi:10.1021/ma00010a013 · Cited by 233 · see citing works

Stereocomplex formation between enantiomeric poly(lactic acid)s. 6. Binary blends from copolymers

Tsuji, H., & Ikada, Y. (1992) · Macromolecules · doi:10.1021/ma00047a024 · Cited by 228 · see citing works

Physically crosslinked dextran hydrogels by stereocomplex formation of lactic acid oligomers: degradation and protein release behavior

de Jong, S. J., Eerdenbrugh, B. V., van Nostrum, C. F., den Bosch, J. J. K.-V., & Hennink, W. E. (2001) · Journal of Controlled Release · doi:10.1016/s0168-3659(01)00228-0 · Cited by 227 · see citing works

Stereocomplex formation between enantiomeric poly(lactic acid)s. 4. Differential scanning calorimetric studies on precipitates from mixed solutions of poly(D-lactic acid) and poly(L-lactic acid)

Tsuji, H., Hyon, S. H., & Ikada, Y. (1991) · Macromolecules · doi:10.1021/ma00020a027 · Cited by 226 · see citing works

An injectable hydrogel formed by in situ cross-linking of glycol chitosan and multi-benzaldehyde functionalized PEG analogues for cartilage tissue engineering

Cao, L., Cao, B., Lu, C., Wang, G., Yu, L., & Ding, J. (2014) · Journal of Materials Chemistry B · doi:10.1039/c4tb01705f · Cited by 216 · see citing works

Functionalized injectable hydrogels for controlled insulin delivery

Huỳnh, Đ. P., Nguyen, M. K., Pi, B. S., Kim, M. S., Chae, S. Y., Lee, K. C., Kim, B. S., Kim, S. W., & Lee, D. S. (2008) · Biomaterials · doi:10.1016/j.biomaterials.2008.02.016 · Cited by 214 · see citing works

Novel Self-assembled Hydrogels by Stereocomplex Formation in Aqueous Solution of Enantiomeric Lactic Acid Oligomers Grafted To Dextran

de Jong, S. J., Smedt, S. C. D., Wahls, M. W. C., Demeester, J., den Bosch, J. J. K.-V., & Hennink, W. E. (2000) · Macromolecules · doi:10.1021/ma992067g · Cited by 214 · see citing works

Influence of Crystallinity and Stereochemistry on the Enzymatic Degradation of Poly(lactide)s

Li, S., & McCarthy, S. (1999) · Macromolecules · doi:10.1021/ma990117b · Cited by 212 · see citing works

FGF-2 and VEGF functionalization of starPEG–heparin hydrogels to modulate biomolecular and physical cues of angiogenesis

Zieris, A., Prokoph, S., Levental, K. R., Welzel, P. B., Grimmer, M., Freudenberg, U., & Werner, C. (2010) · Biomaterials · doi:10.1016/j.biomaterials.2010.07.021 · Cited by 209 · see citing works

Novel in Situ Forming, Degradable Dextran Hydrogels by Michael Addition Chemistry: Synthesis, Rheology, and Degradation

Hiemstra, C., van der Aa, L. J., Zhong, Z., et al. (2007) · Macromolecules · doi:10.1021/ma062468d · Cited by 206 · see citing works

Stereocomplex formation between enantiomeric poly(lactic acid)s. 7. Phase structure of the stereocomplex crystallized from a dilute acetonitrile solution as studied by high-resolution solid-state carbon-13 NMR spectroscopy

Tsuji, H., Horii, F., Nakagawa, M., Ikada, Y., Odani, H., & Kitamaru, R. (1992) · Macromolecules · doi:10.1021/ma00042a011 · Cited by 202 · see citing works

In vitro hydrolysis of blends from enantiomeric poly(lactide)s Part 1. Well-stereo-complexed blend and non-blended films

Tsuji, H. (2000) · Polymer · doi:10.1016/s0032-3861(99)00545-5 · Cited by 200 · see citing works

Thermo-sensitive and biodegradable hydrogels based on stereocomplexed Pluronic multi-block copolymers for controlled protein delivery

Chung, H. J., Lee, Y., & Park, T. G. (2007) · Journal of Controlled Release · doi:10.1016/j.jconrel.2007.12.008 · Cited by 194 · see citing works

Stereocomplex Formation between Enantiomeric Poly(lactic acid)s. 12. Spherulite Growth of Low-Molecular-Weight Poly(lactic acid)s from the Melt

Tsuji, H., & Tezuka, Y. (2004) · Biomacromolecules · doi:10.1021/bm049835i · Cited by 194 · see citing works

Controlled crystal nucleation in the melt-crystallization of poly(l-lactide) and poly(l-lactide)/poly(d-lactide) stereocomplex

Urayama, H., Kanamori, T., Fukushima, K., & Kimura, Y. (2003) · Polymer · doi:10.1016/s0032-3861(03)00583-4 · Cited by 187 · see citing works

Synthesis, Characterization, and Stereocomplex-Induced Gelation of Block Copolymers Prepared by Ring-Opening Polymerization of l ( d )-Lactide in the Presence of Poly(ethylene glycol)

Li, S., & Vert, M. (2003) · Macromolecules · doi:10.1021/ma034734i · Cited by 183 · see citing works

Electrospinning of Poly(lactic acid) Stereocomplex Nanofibers

Tsuji, H., Nakano, M., Hashimoto, M., Takashima, K., Katsura, S., & Mizuno, A. (2006) · Biomacromolecules · doi:10.1021/bm060786e · Cited by 182 · see citing works

Formation of a Novel Heparin-Based Hydrogel in the Presence of Heparin-Binding Biomolecules

Tae, G., Kim, Y.-J., Choi, W., Kim, M.-H., Stayton, P. S., & Hoffman, A. S. (2007) · Biomacromolecules · doi:10.1021/bm0701189 · Cited by 175 · see citing works

Stereocomplex formation of high-molecular-weight polylactide: A low temperature approach

Bao, R., Yang, W. M., Jiang, W., Liu, Z., Xie, B., Yang, M., & Fu, Q. (2012) · Polymer · doi:10.1016/j.polymer.2012.09.043 · Cited by 175 · see citing works

Polylactide Stereocomplexation Leads to Higher Hydrolytic Stability but More Acidic Hydrolysis Product Pattern

Andersson, S. R., Hakkarainen, M., Inkinen, S., Södergård, A., & Albertsson, A. (2010) · Biomacromolecules · doi:10.1021/bm100029t · Cited by 174 · see citing works

Monodisperse Enantiomeric Lactic Acid Oligomers:  Preparation, Characterization, and Stereocomplex Formation

de Jong, S. J., van Dijk-Wolthuis, W. N. E., Kettenes-van den Bosch, J. J., Schuyl, P. J. W., & Hennink, W. E. (1998) · Macromolecules · doi:10.1021/ma980553i · Cited by 172 · see citing works

In Vivo Tissue Response and Degradation Behavior of PLLA and Stereocomplexed PLA Nanofibers

Ishii, D., Ying, T. H., Mahara, A., Murakami, S., Yamaoka, T., Lee, W., & Iwata, T. (2008) · Biomacromolecules · doi:10.1021/bm8009363 · Cited by 169 · see citing works

Stereoblock Polylactides as High-Performance Bio-Based Polymers

Kakuta, M., Hirata, M., & Kimura, Y. (2009) · Journal of macromolecular science. Part C, Reviews in macromolecular chemistry and physics/Journal of macromolecular science. Reviews in macromolecular chemistry and physics · doi:10.1080/15583720902834825 · Cited by 167 · see citing works

In-Situ Formation of Biodegradable Hydrogels by Stereocomplexation of PEG−(PLLA)8 and PEG−(PDLA)8 Star Block Copolymers

Hiemstra, C., Zhong, Z., Li, L., et al. (2006) · Biomacromolecules · doi:10.1021/bm060630e · Cited by 166 · see citing works

Poly( D,L ‐lactic acid‐co‐glycolic acid)‐b‐poly(ethylene glycol)‐b‐poly ( D,L ‐lactic acid‐co‐glycolic acid) triblock copolymer and thermoreversible phase transition in water

Shim, M. S., Lee, H. T., Shim, W. S., Park, I., Lee, H., Chang, T., Kim, S. W., & Lee, D. S. (2002) · Journal of Biomedical Materials Research · doi:10.1002/jbm.10164 · Cited by 161 · see citing works

Rapidly in Situ Forming Biodegradable Robust Hydrogels by Combining Stereocomplexation and Photopolymerization

Hiemstra, C., Zhou, W., Zhong, Z., Wouters, M., & Feijén, J. (2007) · Journal of the American Chemical Society · doi:10.1021/ja072113p · Cited by 158 · see citing works

Anti-tumor drug delivery of pH-sensitive poly (ethylene glycol)-poly (L-histidine-)-poly (L-lactide) nanoparticles

Liu, R., Li, D., He, B., Xu, X., Sheng, M., Lai, Y., Wang, G., & Gu, Z. (2011) · Journal of Controlled Release · doi:10.1016/j.jconrel.2011.02.031 · Cited by 157 · see citing works

Enzymatic Hydrolysis of Poly(lactide)s: Effects of Molecular Weight, l -Lactide Content, and Enantiomeric and Diastereoisomeric Polymer Blending

Tsuji, H., & Miyauchi, S. (2001) · Biomacromolecules · doi:10.1021/bm010048k · Cited by 157 · see citing works

Broad‐Spectrum Antimicrobial and Biofilm‐Disrupting Hydrogels: Stereocomplex‐Driven Supramolecular Assemblies

Li, Y., Fukushima, K., Coady, D. J., Engler, A. C., Liu, S., Huang, Y., Cho, J. S., Guo, Y., Miller, L. S., Tan, J. P. K., et al. (2012) · Angewandte Chemie International Edition · doi:10.1002/anie.201206053 · Cited by 153 · see citing works

Stereocomplex formation between enantiomeric poly(lactic acid). VIII. Complex fibers spun from mixed solution of poly( D ‐lactic acid) and poly( L ‐lactic acid)

Tsuji, H., Ikada, Y., Hyon, S., Kimura, Y., & Kitao, T. (1994) · Journal of Applied Polymer Science · doi:10.1002/app.1994.070510216 · Cited by 152 · see citing works

Stereocomplex formation between enantiomeric poly(lactic acids). 5. Calorimetric and morphological studies on the stereocomplex formed in acetonitrile solution

Tsuji, H., Hyon, S. H., & Ikada, Y. (1992) · Macromolecules · doi:10.1021/ma00037a024 · Cited by 151 · see citing works

Injectable, self-gelling, biodegradable, and immunomodulatory DNA hydrogel for antigen delivery

Nishikawa, M., Ogawa, K., Umeki, Y., et al. (2014) · Journal of Controlled Release · doi:10.1016/j.jconrel.2014.02.001 · Cited by 145 · see citing works

Stereocomplex Formation of High-Molecular-Weight Polylactide Using Supercritical Fluid

Purnama, P., & Kim, S. H. (2009) · Macromolecules · doi:10.1021/ma902536p · Cited by 140 · see citing works

Biodegradable dextran hydrogels crosslinked by stereocomplex formation for the controlled release of pharmaceutical proteins

Hennink, W. E., de Jong, S. J., Bos, G. W., Veldhuis, T. F. J., & van Nostrum, C. F. (2004) · International Journal of Pharmaceutics · doi:10.1016/j.ijpharm.2003.02.002 · Cited by 134 · see citing works

In Situ Cross-Linkable Hydrogel of Hyaluronan Produced via Copper-Free Click Chemistry

Takahashi, A., Suzuki, Y., Suhara, T., et al. (2013) · Biomacromolecules · doi:10.1021/bm4009606 · Cited by 131 · see citing works

Higher-order structures and mechanical properties of stereocomplex-type poly(lactic acid) melt spun fibers

Furuhashi, Y., Kimura, Y., Yoshie, N., & Yamane, H. (2006) · Polymer · doi:10.1016/j.polymer.2006.06.001 · Cited by 127 · see citing works

Poly(l-lactide): 7. Enzymatic hydrolysis of free and restricted amorphous regions in poly(l-lactide) films with different crystallinities and a fixed crystalline thickness

Tsuji, H., & Miyauchi, S. (2001) · Polymer · doi:10.1016/s0032-3861(00)00792-8 · Cited by 127 · see citing works

Unique crystallization behavior of poly(l-lactide)/poly(d-lactide) stereocomplex depending on initial melt states

He, Y., Xu, Y., Wei, J., Fan, Z.-Y., & Li, S. (2008) · Polymer · doi:10.1016/j.polymer.2008.10.028 · Cited by 125 · see citing works

Achieving Micelle Control through Core Crystallinity

Glavas, L., Olsén, P., Odelius, K., & Albertsson, A. (2013) · Biomacromolecules · doi:10.1021/bm401312j · Cited by 123 · see citing works

Mixed Micelle Formation through Stereocomplexation between Enantiomeric Poly(lactide) Block Copolymers

Kim, S. H., Tan, J. P. K., Nederberg, F., Fukushima, K., Yang, Y. Y., Waymouth, R. M., & Hedrick, J. L. (2008) · Macromolecules · doi:10.1021/ma801739x · Cited by 120 · see citing works

Osteogenic differentiation of rat bone marrow stromal cells cultured on Arg–Gly–Asp modified hydrogels without dexamethasone and β-glycerol phosphate

Shin, H., Temenoff, J. S., Bowden, G. C., Zygourakis, K., Farach‐Carson, M. C., Yaszemski, M. J., & Mikos, A. G. (2004) · Biomaterials · doi:10.1016/j.biomaterials.2004.09.050 · Cited by 119 · see citing works

Different enantioselectivity of two types of poly(lactic acid) depolymerases toward poly(l-lactic acid) and poly(d-lactic acid)

Kawai, F., Nakadai, K., Nishioka, E., et al. (2011) · Polymer Degradation and Stability · doi:10.1016/j.polymdegradstab.2011.03.022 · Cited by 118 · see citing works

Simple Approach to Stabilized Micelles Employing Miktoarm Terpolymers and Stereocomplexes with Application in Paclitaxel Delivery

Nederberg, F., Appel, E. A., Tan, J. P. K., Kim, S. H., Fukushima, K., Sly, J., Miller, R. D., Waymouth, R. M., Yang, Y. Y., & Hedrick, J. L. (2009) · Biomacromolecules · doi:10.1021/bm900056g · Cited by 117 · see citing works

Biodegradable hydrogels based on stereocomplex formation between lactic acid oligomers grafted to dextran

de Jong, S. J., Smedt, S. C. D., Demeester, J., et al. (2001) · Journal of Controlled Release · doi:10.1016/s0168-3659(01)00261-9 · Cited by 116 · see citing works

Customizing the Hydrolytic Degradation Rate of Stereocomplex PLA through Different PDLA Architectures

Andersson, S. R., Hakkarainen, M., Inkinen, S., Södergård, A., & Albertsson, A. (2012) · Biomacromolecules · doi:10.1021/bm300196h · Cited by 112 · see citing works

In Situ Gelable Interpenetrating Double Network Hydrogel Formulated from Binary Components: Thiolated Chitosan and Oxidized Dextran

Zhang, H., Qadeer, A., & Chen, W. (2011) · Biomacromolecules · doi:10.1021/bm101192b · Cited by 111 · see citing works

Biodegradable Nanogel Formation of Polylactide-Grafted Dextran Copolymer in Dilute Aqueous Solution and Enhancement of Its Stability by Stereocomplexation

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