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Journal ArticleDOI

Controlled ring-opening polymerization of lactide and glycolide.

05 Oct 2004-Chemical Reviews (American Chemical Society)-Vol. 104, Iss: 12, pp 6147-6176
TL;DR: This work focuses on the characterization of the phytochemical components of Lactide ROP and their role in the regulation of cell reprograming.
Abstract: 23 Stereocontrol of Lactide ROP 6164 231 Isotactic Polylactides 6164 232 Syndiotactic Polylactides 6166 233 Heterotactic Polylactides 6166 3 Anionic Polymerization 6166 4 Nucleophilic Polymerization 6168 41 Mechanistic Considerations 6168 42 Catalysts 6169 421 Enzymes 6169 422 Organocatalysts 6169 43 Stereocontrol of Lactide ROP 6170 44 Depolymerization 6170 5 Cationic Polymerization 6170 6 Conclusion and Perspectives 6171 7 Acknowledgments 6173 8 References and Notes 6173
Citations
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Journal ArticleDOI
TL;DR: This paper presents the design of highly efficient families of “living” polymerization strategies for the synthesis of block, graft, and star polymers through controlled methods for the controlled synthesis of dendritic macromolecules.
Abstract: Modern synthetic methods have revolutionized polymer chemistry through the development of new and powerful strategies for the controlled synthesis of complex polymer architectures. 1-5 Many of these developments were spawned by new classes of transition metal catalysts for the synthesis of new polyolefin microstructures, 5 the design of highly efficient families of “living” polymerization strategies for the synthesis of block, graft, and star polymers, 6-12 controlled methods for the synthesis of dendritic macromolecules, 3,13,14

1,231 citations

Journal ArticleDOI
TL;DR: The analysis of the state of the art in the field reveals the presence of current innovative techniques for scaffolds and material manufacturing that are currently opening the way to prepare biomimetic PLGA substrates able to modulate cell interaction for improved substitution, restoration, or enhancement of bone tissue function.
Abstract: Poly(lactic-co-glycolic) acid (PLGA) has attracted considerable interest as a base material for biomedical applications due to its: (i) biocompatibility; (ii) tailored biodegradation rate (depending on the molecular weight and copolymer ratio); (iii) approval for clinical use in humans by the U.S. Food and Drug Administration (FDA); (iv) potential to modify surface properties to provide better interaction with biological materials; and (v) suitability for export to countries and cultures where implantation of animal-derived products is unpopular. This paper critically reviews the scientific challenge of manufacturing PLGA-based materials with suitable properties and shapes for specific biomedical applications, with special emphasis on bone tissue engineering. The analysis of the state of the art in the field reveals the presence of current innovative techniques for scaffolds and material manufacturing that are currently opening the way to prepare biomimetic PLGA substrates able to modulate cell interaction for improved substitution, restoration, or enhancement of bone tissue function.

1,116 citations


Cites methods from "Controlled ring-opening polymerizat..."

  • ...Usually, by the cited ring-opening polymerization technique, randomly distributed atactic or syndiotactic PLGA is obtained as reported in detail by Dechy-Cabaret [26], depending both on the monomer involved and on the course of the polymerization reaction....

    [...]

Journal ArticleDOI
TL;DR: In this article, the ring-opening polymerization of cyclic monomers is used as a representative polymerization process to illustrate some of the features of organic catalysts and initiators and compare them to metal-based approaches.
Abstract: Organocatalysis offers a number of opportunities in polymer synthesis and was among the earliest methods of catalyzing the synthesis of polyesters. In the following Perspective we attempt to highlight the opportunities and challenges in the use of organic molecules as catalysts or initiators for polymerization reactions. The ring-opening polymerization of cyclic monomers is used as a representative polymerization process to illustrate some of the features of organic catalysts and initiators and to compare them to metal-based approaches. The convergence of convenience, functional group tolerance, fast rates, and selectivities will continue to drive innovations in polymerization catalysis, and it is our perspective that organocatalysis will continue to play an important role in these developments.

749 citations

Journal ArticleDOI
TL;DR: This tutorial review focuses on the use of metal-based complexes for the stereoselective ROP of rac-LA and rac-BBL.
Abstract: Synthesis of aliphatic polyesters has been studied intensively due to their biocompatible and biodegradable properties and their potential applications in medical and agricultural fields. There has been particular emphasis over the past decade on the synthesis of discrete, well-characterized complexes that are active polymerization initiators for the ring-opening polymerization (ROP) of lactide (LA) and β-butyrolactone (BBL) to give, respectively, poly(lactide) (PLA) and poly(3-hydroxybutyrate) (PHB). These recent advances in catalyst design have led to a variety of polyester microstructures. This tutorial review focuses on the use of metal-based complexes for the stereoselective ROP of rac-LA and rac-BBL.

733 citations

Journal ArticleDOI
TL;DR: In this paper, a review describes the development of ring-opening polymerization of cyclic esters using main group metal complexes as catalysts/initiators, and the complexes described here are classified according to metal groups.

727 citations

References
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Journal ArticleDOI
TL;DR: N-Heterocyclic carbenes have become universal ligands in organometallic and inorganic coordination chemistry as mentioned in this paper, and they not only bind to any transition metal, be it in low or high oxidation states, but also to main group elements such as beryllium, sulfur, and iodine.
Abstract: N-Heterocyclic carbenes have become universal ligands in organometallic and inorganic coordination chemistry. They not only bind to any transition metal, be it in low or high oxidation states, but also to main group elements such as beryllium, sulfur, and iodine. Because of their specific coordination chemistry, N-heterocyclic carbenes both stabilize and activate metal centers in quite different key catalytic steps of organic syntheses, for example, C-H activation, C-C, C-H, C-O, and C-N bond formation. There is now ample evidence that in the new generation of organometallic catalysts the established ligand class of organophosphanes will be supplemented and, in part, replaced by N-heterocyclic carbenes. Over the past few years, this chemistry has been the field of vivid scientific competition, and yielded previously unexpected successes in key areas of homogeneous catalysis. From the work in numerous academic laboratories and in industry, a revolutionary turning point in oraganometallic catalysis is emerging.

3,388 citations

Journal ArticleDOI
TL;DR: Based on the above mechanism, various potential applications of nanoparticles for delivery of therapeutic agents to the cells and tissue are discussed.

3,269 citations

Journal ArticleDOI
TL;DR: Polylactic acid is proving to be a viable alternative to petrochemical-based plastics for many applications It is produced from renewable resources and is biodegradable, decomposing to give H2O, CO2, and humus, the black material in soil as mentioned in this paper.
Abstract: Polylactic acid is proving to be a viable alternative to petrochemical-based plastics for many applications It is produced from renewable resources and is biodegradable, decomposing to give H2O, CO2, and humus, the black material in soil In addition, it has unique physical properties that make it useful in diverse applications including paper coating, fibers, films, and packaging (see Figure)

2,537 citations

Journal ArticleDOI
TL;DR: Kevin Shakesheff investigates new methods of engineering polymer surfaces and the application of these engineered materials in drug delivery and tissue engineering.
Abstract: s, and 360 patents, and edited 12 books. He has also received over 80 major awards including the Gairdner Foundation International Award, Lemelson-MIT prize, ACS’s Applied Polymer Science and Polymer Chemistry Awards, AICHE’s Professional Progress, Bioengineering, Walker and Stine Materials Science and Engineering Awards. In 1989, Dr. Langer was elected to the Institute of Medicine of the National Academy of Sciences, and in 1992 he was elected to both the National Academy of Engineering and the National Academy of Sciences. He is the only active member of all three National Academies. Kevin Shakesheff was born in Ashington, Northumberland, U.K., in 1969. He received his Bacheclor of Pharmacy degree from the University of Nottingham in 1991 and a Ph.D. from the same institution in 1995. In 1996 he became a NATO Postdoctoral Fellow at MIT, Department of Chemical Engineering. He is currently an EPSRC Advanced Fellow at the School of Pharmaceutical Sciences, The University of Nottingham. His research group investigates new methods of engineering polymer surfaces and the application of these engineered materials in drug delivery and tissue engineering. 3182 Chemical Reviews, 1999, Vol. 99, No. 11 Uhrich et al.

2,532 citations

Journal ArticleDOI
TL;DR: In this paper, the authors focus on properties of biodegradable polymers which make them ideally suited for orthopedic applications where a permanent implant is not desired, and an overview of biocompatibility and approved devices of particular interest in orthopedics are also covered.

2,526 citations