ABSTRACT VAID, RADHIKA Chemical and Thermal Degradation of Fiber Forming Aliphatic Polyesters

Total Page:16

File Type:pdf, Size:1020Kb

ABSTRACT VAID, RADHIKA Chemical and Thermal Degradation of Fiber Forming Aliphatic Polyesters ABSTRACT VAID, RADHIKA Chemical and Thermal Degradation of Fiber Forming Aliphatic Polyesters. (Under the direction of Dr. Martin W. King and Dr. Melissa A. Pasquinelli). Bioresorbable polymers are employed for many applications in the biotechnology, medical device, and pharmaceutical industries on account of their biocompatibility and biodegradability. This makes them viable candidates for treating acute injuries and chronic diseases through tissue engineering scaffolds, wound dressings, resorbable surgical sutures and drug delivery systems. Thus, it becomes important to ensure that when polymers have been processed or fabricated into a particular shape, size and form that they have the desired degradation profile for the application they are designed for. The polymer's processing conditions play a significant role in determining the degradation mechanism which is controlled by the structure property relationship and hence the bioresorbable properties. In addition, the in vivo environmental factors such as pH and enzymes have a significant impact on the degradation profile and clinical performance of the polymer when implanted in the body as a resorbable device. In the past there have been many studies evaluating resorbable polymers, like polylactic acid (PLA), to understand the degradation behavior for biomedical applications. But gaps still exist in our understanding of the degradation process and the reaction mechanism of a wide range of established resorbable polymers. In addition, there is limited scientific literature on the degradation behavior of other newly developed bioresorbable polymers, like poly-4-hydroxybutyrate (P4HB), and how they compare with established polymers. For my doctoral research study, I have evaluated different bioresorbable polymers in the category of aliphatic polyesters, including polycaprolactone (PCL) and polyglycolic acid (PGA) in addition to PLA and P4HB, with the goal of understanding their degradation mechanism, their resorption profile and any implications on their properties critical to their polymer performance. To accomplish this, I have used both experiments and computational techniques and have attempted to establish correlations between these two approaches so that the methods developed are applicable to other polymers. Sometimes in experiments, details at the molecular level critical to polymer degradation and their use are omitted or missed, such as reaction mechanisms and the production of by-products. In the initial studies, I have evaluated the degradation properties as a function of pH for both PLA and P4HB. P4HB is an attractive candidate for use as a surgical suture because it is an elastic thermoplastic that is biodegradable, biocompatible, insoluble in water and nontoxic. It also has a high degree of polymerization and thus has potential for high strength applications. For the PLA and P4HB degradation studies using both experimental and simulation techniques, the degradation conditions were selected so as to mimic normal body temperature and the pH conditions present at various locations in the human body. Then, in order to explore the details of the hydrolytic degradation mechanism at the molecular-level, molecular dynamics (MD) simulations were performed using reaxFF and density functional theory (DFT) calculations. In a second set of studies, I also performed experiments to analyze the effect of the proteinase K enzyme under different pH conditions on the degradation behavior of P4HB. Finally, thermal degradation was studied for four aliphatic polyesters, using both experiments and simulations. The results were correlated in terms of the activations energies and thermal degradation profiles. The findings for hydrolytic degradation from both experiments and simulations illustrated that a faster rate of degradation occurred for PLA in alkaline conditions, whereas for P4HB degradation was enhanced under acidic conditions. Furthermore, similar behavior, but to lesser extent, was observed for the enzymatic degradation of P4HB in the presence of proteinase K. Lastly, thermal degradation using both experimental and simulation techniques revealed similar degradation profiles and activation energies for all four aliphatic polyesters. In summary, it is important to note that this study is unique and one of a kind. It puts forward a methodology where the simulations can be used as a tool to study polymer degradation in combination with experiments, and by taking this approach it is possible to clarify our understanding of the degradation process, and now we can shortlist polymer candidates based on the results of simulations before proceeding with experimental work and material processing. © Copyright 2020 by Radhika Vaid All Rights Reserved Chemical and Thermal Degradation of Fiber Forming Aliphatic Polyesters by Radhika Vaid A dissertation submitted to the Graduate Faculty of North Carolina State University in partial fulfillment of the requirements for the degree of Doctor of Philosophy Fiber and Polymer Science and Materials Science and Engineering Raleigh, North Carolina 2020 APPROVED BY: _______________________________ _______________________________ Dr. Martin W. King Dr. Melissa A. Pasquinelli Committee Co-Chair Committee Co-Chair _______________________________ _______________________________ Dr. Ericka Ford Dr. Yaroslava Yingling _______________________________ _______________________________ Dr. Albena Ivanisevic Dr. Nathalie Lavoine DEDICATION Dedicated to my parents, Neelam Vaid and Pradeep Kumar Vaid, and my sister Pooja (a special gift of God to us) ii BIOGRAPHY Radhika Vaid, was born in Himachal Pradesh, India on September 1st 1988. Having been guided by her elder sister, Dr. Rajni Vaid Puri, she pursued her studies in the less popular field of textiles engineering. During her bachelor's degree she was amazed by exploring a multitude of applications of textiles, so after her bachelors from Jawahar Lal Nehru Government Engineering College, Sundernagar, H.P, she continued to pursue and obtain her master of technology degree in Fiber Science and Technology from the Indian Institute of Technology, Delhi. Thereafter, she worked as a fiber and polymer scientist at Aditya Birla Science and Technology Company Pvt. Ltd., India. After working there for three years she came to North Carolina State University to study for a doctoral degree and to follow her dream to be a polymer scientist. At present, Radhika is enrolled as a candidate for the Ph.D. degree in Fiber and Polymer Science with a co-major in Materials Science and Engineering. Radhika has an inclination and enthusiasm for polymers; to study them, unfurl them and apply them to novel applications. iii ACKNOWLEDGMENTS This journey towards the accomplishment of my Ph.D. is the result of support and continuous motivation from many incredible people in my life. First and foremost, I would like to thank my advisors, Dr. Melissa A. Pasquinelli and Dr. Martin W. King, for their unconditional support and constant push throughout the past four and half years. These two have guided me both technically and emotionally through the storm of failure and winds of success. If it wasn’t for these two, I am sure I would have been lost and disheartened in this journey of earning a doctoral degree. Dr. King, my academic father, as I always address him, has virtually been there at my back whenever I turned around in a moment of despair, telling me with a sparkling smile, "Keep going Radhika. Hang in there. I know you can do it". At times this has pumped and motivated me to have confidence in myself and my research. Dr. King with scientific experience of almost double my age has relentlessly ensured that I attend conferences, learn from others and apply the new knowledge to improve my research. On the other hand, Dr. Pasquinelli has always been a female icon for me and has guided me and challenged me to do my best. She has been there for me to make life easier and overcome whatever barriers I have faced technically and administratively to undertake and obtain a co-major within my Ph.D program. I would rather say that she has been my guiding light throughout my Ph.D. and has helped me to improve my presentation and communication skills. Now when I look back, these two pillars have always shown their confidence and trust in me, and have fostered this journey for achieving my best. Furthermore, I would like to extend my gratitude to the laboratory staff at the Wilson College of Textiles, the Analytical Instrumentation Facility (AIF), the Department of Material Science & Engineering (MSE) and at Donghua University for their support to accomplish the technical objectives of my Ph.D. research project. The people who have assisted me have been iv more than just staff to me. They have been prepared to go out of their way and help me whenever I have asked. I am especially thankful to Birgit Andersen and Joyce Cole for being kind and helpful to me whenever I have needed. Thank you for lifting my morale at times and keeping me motivated. In addition, I would like to extend my appreciation to my committee members for their role in giving me time and making sure that gaps in my research are addressed. I would personally like to thank Dr. Ericka Ford for her patience whenever I arrived uninvited in her office to discuss my research. Her insights in the analysis for DSC and TGA have been particularly helpful in understanding the property changes during degradation of the polymers I studied. In addition, Dr. Yarasolava Yingling have rendered her expertise to understand the degradation of polymers using simulations and how to extract meaningful information from the analysis. Further, I would like to thank Dr. Albena Ivanisevic for being resourceful and directing me to the right people for any technical support and information needed for my research. Lastly, I would like to also acknowledge the role of my Graduate School representative (GSR), initially Dr. Sophia Kathariou for being understanding, kind and supportive. I am sorry for the loss she has incurred and sorry for the fact that she cannot be with us for my final oral examination. To replace her, I appreciate Dr. Nathalie Lavoine agreeing to be my committee member and GSR at such short notice.
Recommended publications
  • The Development of a Biodegradable Drug Delivery System for Orthopedic Infection in the Horse
    Iowa State University Capstones, Theses and Retrospective Theses and Dissertations Dissertations 1-1-1999 The development of a biodegradable drug delivery system for orthopedic infection in the horse : in vitro and in vivo biocompatibility and gentamicin elution characteristics Axel Friedrich Sondhof Iowa State University Follow this and additional works at: https://lib.dr.iastate.edu/rtd Recommended Citation Sondhof, Axel Friedrich, "The development of a biodegradable drug delivery system for orthopedic infection in the horse : in vitro and in vivo biocompatibility and gentamicin elution characteristics" (1999). Retrospective Theses and Dissertations. 17799. https://lib.dr.iastate.edu/rtd/17799 This Thesis is brought to you for free and open access by the Iowa State University Capstones, Theses and Dissertations at Iowa State University Digital Repository. It has been accepted for inclusion in Retrospective Theses and Dissertations by an authorized administrator of Iowa State University Digital Repository. For more information, please contact [email protected]. The development of a biodegradable drug delivery system for orthopedic infection in the horse: Jn vitro and in vivo biocompatibility and gentamicin elution characteristics by Axel Friedrich Sondhof A thesis submitted to the graduate faculty in partial fulfillment of the requirements for the degree of MASTER OF SCIENCE Major: Veterinary Clinical Sciences (Veterinary Surgery) Major Professor: Larry C. Booth Iowa State University Ames, Iowa 1999 ii Graduate College Iowa State University This is to certify that the Master's thesis of Axel Friedrich Sondhof has met the thesis requirements oflowa State University Signatures have been redacted for privacy iii TABLE OF CONTENTS CHAPTER 1. GENERAL INTRODUCTION Thesis Organization Introduction Literature Review 2 CHAPTER 2.
    [Show full text]
  • Solvent Induced Phase Inversion-Based in Situ Forming Controlled Release Drug Delivery Implants
    Journal of Controlled Release 176 (2014) 8–23 Contents lists available at ScienceDirect Journal of Controlled Release journal homepage: www.elsevier.com/locate/jconrel Review Solvent induced phase inversion-based in situ forming controlled release drug delivery implants Raghu Raj Singh Thakur ⁎, Hannah L. McMillan, David S. Jones Drug Delivery and Biomaterials Group, School of Pharmacy, Medical Biology Centre Queen's University Belfast, 97 Lisburn Road, Belfast BT9 7BL, UK article info abstract Article history: In situ forming (ISF) drug delivery implants have gained tremendous levels of interest over the last few decades. Received 19 September 2013 This is due to their wide range of biomedical applications such as in tissue engineering, cell encapsulation, Accepted 19 December 2013 microfluidics, bioengineering and drug delivery. Drug delivery implants forming upon injection has shown a Available online 27 December 2013 range of advantages which include localized drug delivery, easy and less invasive application, sustained drug action, ability to tailor drug delivery, reduction in side effects associated with systemic delivery and also improved patient Keywords: compliance and comfort. Different factors such as temperature, pH, ions, and exchange of solvents are involved in in In situ forming implants Solvent induced phase inversion implants situ implant formation. This review especially focuses on ISF implants that are formed through solvent induced Controlled release phase inversion (SPI) technique. The article critically reviews and compares a wide range of polymers, solvents, Sustained release and co-solvents that have been used in SPI implant preparation for control release of a range of drug molecules. Drug delivery Major drawback of SPI systems has been their high burst release.
    [Show full text]
  • WO 2014/078014 A2 22 May 2014 (22.05.2014) P O P C T
    (12) INTERNATIONAL APPLICATION PUBLISHED UNDER THE PATENT COOPERATION TREATY (PCT) (19) World Intellectual Property Organization International Bureau (10) International Publication Number (43) International Publication Date WO 2014/078014 A2 22 May 2014 (22.05.2014) P O P C T (51) International Patent Classification: (81) Designated States (unless otherwise indicated, for every C07D 307/06 (2006.01) kind of national protection available): AE, AG, AL, AM, AO, AT, AU, AZ, BA, BB, BG, BH, BN, BR, BW, BY, (21) International Application Number: BZ, CA, CH, CL, CN, CO, CR, CU, CZ, DE, DK, DM, PCT/US2013/065916 DO, DZ, EC, EE, EG, ES, FI, GB, GD, GE, GH, GM, GT, (22) International Filing Date: HN, HR, HU, ID, IL, IN, IR, IS, JP, KE, KG, KN, KP, KR, 2 1 October 2013 (21 .10.201 3) KZ, LA, LC, LK, LR, LS, LT, LU, LY, MA, MD, ME, MG, MK, MN, MW, MX, MY, MZ, NA, NG, NI, NO, NZ, (25) Filing Language: English OM, PA, PE, PG, PH, PL, PT, QA, RO, RS, RU, RW, SA, (26) Publication Language: English SC, SD, SE, SG, SK, SL, SM, ST, SV, SY, TH, TJ, TM, TN, TR, TT, TZ, UA, UG, US, UZ, VC, VN, ZA, ZM, (30) Priority Data: ZW. 61/726,294 14 November 2012 (14. 11.2012) US 61/772,602 5 March 2013 (05.03.2013) US (84) Designated States (unless otherwise indicated, for every 61/823,5 18 15 May 2013 (15.05.2013) us kind of regional protection available): ARIPO (BW, GH, 61/834,974 14 June 2013 (14.06.2013) us GM, KE, LR, LS, MW, MZ, NA, RW, SD, SL, SZ, TZ, UG, ZM, ZW), Eurasian (AM, AZ, BY, KG, KZ, RU, TJ, (71) Applicant: METABOLIX, INC.
    [Show full text]
  • Biodegradable Materials for Bone Defect Repair Shuai Wei1, Jian-Xiong Ma1, Lai Xu2, Xiao-Song Gu2* and Xin-Long Ma1*
    Wei et al. Military Medical Research (2020) 7:54 https://doi.org/10.1186/s40779-020-00280-6 REVIEW Open Access Biodegradable materials for bone defect repair Shuai Wei1, Jian-Xiong Ma1, Lai Xu2, Xiao-Song Gu2* and Xin-Long Ma1* Abstract Compared with non-degradable materials, biodegradable biomaterials play an increasingly important role in the repairing of severe bone defects, and have attracted extensive attention from researchers. In the treatment of bone defects, scaffolds made of biodegradable materials can provide a crawling bridge for new bone tissue in the gap and a platform for cells and growth factors to play a physiological role, which will eventually be degraded and absorbed in the body and be replaced by the new bone tissue. Traditional biodegradable materials include polymers, ceramics and metals, which have been used in bone defect repairing for many years. Although these materials have more or fewer shortcomings, they are still the cornerstone of our development of a new generation of degradable materials. With the rapid development of modern science and technology, in the twenty-first century, more and more kinds of new biodegradable materials emerge in endlessly, such as new intelligent micro- nano materials and cell-based products. At the same time, there are many new fabrication technologies of improving biodegradable materials, such as modular fabrication, 3D and 4D printing, interface reinforcement and nanotechnology. This review will introduce various kinds of biodegradable materials commonly used in bone defect repairing, especially the newly emerging materials and their fabrication technology in recent years, and look forward to the future research direction, hoping to provide researchers in the field with some inspiration and reference.
    [Show full text]
  • (12) United States Patent (10) Patent No.: US 8,133,968 B2 Alkatout Et Al
    USOO8133968B2 (12) United States Patent (10) Patent No.: US 8,133,968 B2 Alkatout et al. (45) Date of Patent: Mar. 13, 2012 (54) POLY(ORTHOESTER) POLYMERS, AND 5,030,457 A 7/1991 Ng et al. METHODS OF MAKING AND USING SAME 5,108,755 A 4, 1992 Daniels et al. 5,211,951 A 5/1993 Sparer et al. 5,254,345 A 10/1993 Pogany et al. (75) Inventors: Julie A. Alkatout, Minneapolis, MN 5,336,505 A 8/1994 Ng et al. (US); Michael Eric Benz, Ramsey, MN 5,374,681 A 12/1994 Kroner et al. (US); Randall V. Sparer, Andover, MN 5,461,140 A 10, 1995 Heller et al. 5,587,507 A 12/1996 Kohnet al. (US) 5,618,563 A 4/1997 Berde et al. 5,700,485 A 12/1997 Berde et al. (73) Assignee: Medtronic, Inc., Minneapolis, MN (US) 5,747,058 A 5/1998 Tipton et al. 5,747,060 A 5/1998 Sackler et al. (*) Notice: Subject to any disclaimer, the term of this 5,824,343 A 10/1998 Ng et al. patent is extended or adjusted under 35 5,837,228 A 11/1998 Shih et al. U.S.C. 154(b) by 0 days. 5,919,473 A 7/1999 Elkhoury 5,939,453 A 8, 1999 Heller et al. 5,942,241 A 8, 1999 Chasin et al. (21) Appl. No.: 12/968,004 5,968,542 A 10/1999 Tipton 5,968,543 A 10, 1999 Heller et al. (22) Filed: Dec.
    [Show full text]
  • This Article Appeared in a Journal Published by Elsevier. the Attached Copy Is Furnished to the Author for Internal Non-Commerci
    This article appeared in a journal published by Elsevier. The attached copy is furnished to the author for internal non-commercial research and education use, including for instruction at the authors institution and sharing with colleagues. Other uses, including reproduction and distribution, or selling or licensing copies, or posting to personal, institutional or third party websites are prohibited. In most cases authors are permitted to post their version of the article (e.g. in Word or Tex form) to their personal website or institutional repository. Authors requiring further information regarding Elsevier’s archiving and manuscript policies are encouraged to visit: http://www.elsevier.com/copyright Author's personal copy Biomaterials 30 (2009) 1657–1664 Contents lists available at ScienceDirect Biomaterials journal homepage: www.elsevier.com/locate/biomaterials A unified mathematical model for the prediction of controlled release from surface and bulk eroding polymer matrices Sam N. Rothstein a,b, William J. Federspiel a,b,c,e, Steven R. Little a,b,d,e,* a Department of Chemical Engineering, University of Pittsburgh, Pittsburgh, PA 15203, USA b McGowan Institute for Regenerative Medicine, University of Pittsburgh, Pittsburgh, PA 15203, USA c Department of Surgery, University of Pittsburgh, Pittsburgh, PA 15203, USA d Department of Immunology, University of Pittsburgh, Pittsburgh, PA 15203, USA e Department of Bioengineering, University of Pittsburgh, Pittsburgh, PA 15203, USA article info abstract Article history: A unified model has been developed to predict release not only from bulk eroding and surface eroding Received 13 October 2008 systems but also from matrices that transition from surface eroding to bulk eroding behavior during the Accepted 1 December 2008 course of degradation.
    [Show full text]
  • Can Biodegradable Polymer DES Be G Y Better Than 2Nd Generation DES?
    Can Biodeggyradable Polymer DES Be Better than 2nd Generation DES? G. Nakazawa, MD Tokai Univ. Japan CVCV--HILLsHILLs Receiving Research Grant From Abbott Vascul ar Japan Boston Scientific Japan Medtronic Vascular Japan Cordis Johnson & Johnson Terumo Corp. Biosensors Japan Adv isory Con trac t With Abbott Vascular Japan Terumo Corp. Components of DES Metal/Design Thick struts ~ 81-140 microns Polymer Drugs Non-erodable Sirolimus-135µg Erodable Drug and Release kinetics Everolimus – 100 µg Determine Paclitaxel- 80 µg Antiproliferative effects Biolimus A9 – 225 µg Localized Hypersensitivity Reaction in Cyp her LAD: Cypher (17months) RCA: Cypher (17months) A B E F C D Nakazawa, G et al. J Am Coll Cardiol 2011: 57(4).390-8 Long Term Safety : Future Directions LLonongg--TSftfDESFtDitiTTSftfDESFtDitiTermerm SSaaffeettyy ooff DESDES:: FFuuttureure DiDirecrectitionsons Asymmetric Biodegradable No Polymer Polymer No DrugDrug General criteria for selecting a pollymer for use as bioma ter ia l • Does not evoke an inflammatory/toxic response, disproportionate to its beneficial effect • Is metabolized in the body after fulfilling its purpose, leave no trace • Is easily processed into the final product form • Has acceptable shelf life • Is easily sterilized Middleton JC and Tipton AJ. Biomaterials 2000;21:2335 Syygynthetic Biodegradable Polymers • Poly(lactide) (PLA) • Poly(glycolide) (PGA) • Poly(glycolic-co-lactic acid) (PLGA) • Pl(Poly(e-caprolactone)(PCL)) (PCL) • Poly(dioxanone) (PDS) • Poly(glycolide-co-trimethylene carbonate) (PGA-TMC) Degradation
    [Show full text]
  • (12) United States Patent (10) Patent No.: US 8,956,642 B2 Hobot Et Al
    USOO8956642B2 (12) United States Patent (10) Patent No.: US 8,956,642 B2 Hobot et al. (45) Date of Patent: Feb. 17, 2015 (54) BUPIVACAINE FORMULATION INA 4,735,804 A 4, 1988 Caldwell et al. POLYORTHOESTER CARRIER 4,758.436 A 7, 1988 Caldwell et al. 4,764,364 A 8, 1988 Heller et al. 4,765,973 A 8, 1988 Heller (75) Inventors: Christopher M. Hobot, Tonka Bay, MN 4,767,627 A 8, 1988 Caldwell et al. (US); Michael E. Benz, Ramsey, MN 4,780,319 A 10/1988 Zentner et al. (US); Keith R. Hildebrand, Houlton, 4,855,132 A 8, 1989 Heller et al. WI (US); Bryant J. Pudil, Plymouth, 4,898,928 A 2f1990 Heller et al. MN (US) 4.946,931 A 8, 1990 Heller et al. 4,957,998 A 9, 1990 Heller et al. (73) Assignee: Medtronic, Inc., Minneapolis, MN (US) 5,030,4575,013,821 A 7,5/1991 1991 N.Heller s et al. 5,108,755 A 4, 1992 Daniels et al. (*) Notice: Subject to any disclaimer, the term of this 5,211,951 A 5/1993 Sparer et al. patent is extended or adjusted under 35 35. A 1. E. gyet al. U.S.C. 154(b) by 1112 days. 5,374,681.- - w A 12/1994 Kronerget al. et al. 5,461,140 A 10, 1995 Heller et al. (21) Appl. No.: 12/426,005 5.487,739 A 1/1996 Aebischer et al. 5,587,507 A 12/1996 Kohnet al. (22) Filed: Apr. 17, 2009 5,618,563 A 4/1997 Berde et al.
    [Show full text]
  • (12) United States Patent (10) Patent No.: US 6,623,730 B1 Williams Et Al
    USOO662373OB1 (12) United States Patent (10) Patent No.: US 6,623,730 B1 Williams et al. (45) Date of Patent: Sep. 23, 2003 (54) THERAPEUTIC USES OF POLYMERS AND Byrom, “Miscellaneous Biomaterials,” in Biomaterials (D. OLGOMERS COMPRISING Byrom, ed.) pp. 333-359 (MacMillan Publishers, London GAMMA-HYDROXYBUTYRATE 1991). Colombo, et al., “Involvement of GABA(A) and GABA(B) (75) Inventors: Simon F. Williams, Sherborn, MA receptors in the mediation of discriminative Stimulus effects (US); David P. Martin, Arlington, MA of gamma-hydroxybutyric acid.” Physiology & Behavior (US) 64:293–302 (1998). Dubois, et al., “Macromolecular Engineering of Polylac (73) Assignees: Tepha, Inc., Cambridge, MA (US); tones and Polylactides. 12. Study of the Depolymerization Metabolix, Inc., Cambridge, MA (US) Reactions of Poly (e-caprolactone) with Functional Alumi (*) Notice: Subject to any disclaimer, the term of this num Alkoxide End Groups.” Macromolecules 26:4407-12 patent is extended or adjusted under 35 (1993). U.S.C. 154(b) by 99 days. Entholzner, et al., “EEG changes during Sedation with gamma-hydroxybutyric acid.” Anaesthesist 44:345-350 (21) Appl. No.: 09/661,948 (1995). Gerra, et al., “Flumazenil effects on growth hormone (22) Filed: Sep. 14, 2000 response to gamma-hydroxybutyric acid.” International Related U.S. Application Data Clinical Psychopharmacology 9:211-215 (1994). (60) Provisional application No. 60/182,371, filed on Feb. 14, Gross, et al., “Polymerization if B-monosubstituted-b-pro 2000, and provisional application No. 60/153.844, filed on piolactones using trialkylaminimum-water catalytic SyS Sep. 14, 1999. tems and polymer characterization,” Macromolecules 21:2657–2668 (1988). (51) Int.
    [Show full text]
  • {Replace with the Title of Your Dissertation}
    Reductively Degradable Polymeric Biomaterials A DISSERTATION SUBMITTED TO THE FACULTY OF UNIVERSITY OF MINNESOTA BY Walter Eugene Partlo III IN PARTIAL FULFILLMENT OF THE REQUIREMENTS FOR THE DEGREE OF DOCTOR OF PHILOSOPHY T. Andrew Taton, Adviser January, 2015 © Walter Eugene Partlo III Acknowledgements I would like to thank the following people for their contribution to the research reported in this thesis and for their support during my time at the University of Minnesota: T. Andrew Taton for his advice and guidance throughout my graduate career. His flexibility was crucial to growth both as a scientist and a person during my graduate school tenure. All of the members of the Taton research group that have made this an amazing experience that has taught me much. Thank you Alexi Young for your friendship and help in and out of graduate school. Thank you to Chandru Ramasubramian, and Amanda Maxwell for all of your editorial and synthetic talents, and allowing me to use both of you so often as my verbal sounding board. Thanks also to Jun Sung Kang, Kevin Landmark, Jon Helander, Brady Jones, Santosh Khatwani, Ara Celi DiCostanzo, Isaac Marks, Tony Reuter, and Andrew Cleland for your help, company, and just always being awesome labmates. Wayland Noland for his guidance and for giving me enough leash to make being a teaching assistant for 6 years a truly rewarding and enlightening experience. To all of the chemistry department community for the overwhelming support following my accident last summer. An extra special thanks to Chuck Tomlinson for helping me navigate the administrivia that followed.
    [Show full text]
  • Functionalizable Biodegradable Polyesters For
    FUNCTIONALIZABLE BIODEGRADABLE POLYESTERS FOR DRUG DELIVERY APPLICATIONS A Dissertation Presented to The Graduate Faculty of The University of Akron In Partial Fulfillment of the Requirements for the Degree Doctor of Philosophy Abhishek Banerjee May, 2012 FUNCTIONALIZABLE BIODEGRADABLE POLYESTERS FOR DRUG DELIVERY APPLICATIONS Abhishek Banerjee Dissertation Approved: Accepted: ______________________________ ______________________________ Advisor Department Chair Dr. Coleen Pugh Dr. Ali Dhinojwala ______________________________ ______________________________ Committee Chair Dean of the College Dr. Li Jia Dr. Stephen Cheng ______________________________ ______________________________ Committee Member Dean of the Graduate School Dr. Abraham Joy Dr. George R. Newkome ______________________________ ______________________________ Committee Member Date Dr. William J. Landis ______________________________ Committee Member Dr. Yang H. Yun ii ABSTRACT Current biodegradable polymers, like poly(lactic acid) (PLA), poly(glycolic acid) (PGA) and their copolymers (PLGA) do not have functionalities on their backbones. Such biodegradable polymer systems are therefore not able to covalently attach drugs or other therapeutic molecules, which could be useful for making drug delivery devices. Instead, the therapeutic molecules must be physically entrapped into these polymers, either by forming micelles or by nano-encapsulation, thereby limiting their loading capacity. Our research deals with the polyesterification of 2-bromo-3-hydroxypropanoic acid which is
    [Show full text]
  • CHARACTERIZATION of ELECTROSPUN DLPLGA NANOFIBERS for a DRUG DELIVERY SYSTEM for INTRACRANIAL TUMORS and Avms
    Copyright Warning & Restrictions The copyright law of the United States (Title 17, United States Code) governs the making of photocopies or other reproductions of copyrighted material. Under certain conditions specified in the law, libraries and archives are authorized to furnish a photocopy or other reproduction. One of these specified conditions is that the photocopy or reproduction is not to be “used for any purpose other than private study, scholarship, or research.” If a, user makes a request for, or later uses, a photocopy or reproduction for purposes in excess of “fair use” that user may be liable for copyright infringement, This institution reserves the right to refuse to accept a copying order if, in its judgment, fulfillment of the order would involve violation of copyright law. Please Note: The author retains the copyright while the New Jersey Institute of Technology reserves the right to distribute this thesis or dissertation Printing note: If you do not wish to print this page, then select “Pages from: first page # to: last page #” on the print dialog screen The Van Houten library has removed some of the personal information and all signatures from the approval page and biographical sketches of theses and dissertations in order to protect the identity of NJIT graduates and faculty. ABSTRACT CHARACTERIZATION OF ELECTROSPUN DLPLGA NANOFIBERS FOR A DRUG DELIVERY SYSTEM FOR INTRACRANIAL TUMORS AND AVMs by Kimberly A. Griswold Eecosiig ocesses ay eecic ies o a oyme souio i oe o ouce sas o oyme i e aoscae age ese oyme ies ae maiuae
    [Show full text]