Home Preparation of poly(sebacic anhydride) and polylactic acid pills used as drug carrier for levofloxacin controlled release
Article
Licensed
Unlicensed Requires Authentication

Preparation of poly(sebacic anhydride) and polylactic acid pills used as drug carrier for levofloxacin controlled release

  • Zhuan Zhang , Liao-Bing Chen EMAIL logo , Jie Gao , Feng Bao , Jing Yin , Biao Chen , Hui Wang , Yun Chen and Liang Shang
Published/Copyright: August 30, 2013
Become an author with De Gruyter Brill

Abstract

A biodegradable local drug release system consisting of poly(sebacic anhydride) and polylactic acid was developed for the purpose of osteomyelitis therapy. Five kinds of poly(sebacic anhydride) with different molecular weights were synthesized, and levofloxacin was chosen as a model antibacterial drug in the in vitro release within 38 days. As the molecular weight of poly(sebacic anhydride) increased, the melting point (Tm) of the matrices increased and the surface morphology became smoother. Consequently, the initial burst effect was reduced and the release rate significantly decreased. In addition, the kinetics of pills containing poly(sebacic anhydride) (Mw=13,000) were close to zero order release. The release profile reveals that the thermodynamic properties and morphology of these matrices, which are affected by the molecular weight, are essential for developing controllable delivery systems. The drug release rate could be easily controlled by the molecular weight of the poly(sebacic anhydride). Finally, these prospective results allow the biodegradable controlled release systems to be employed as carriers for the treatment of chronic osteomyelitis, as well as for other medical applications.


Corresponding author: Liao-Bing Chen, Department of Orthopedic Surgery, Zhongnan Hospital of Wuhan University, Donghu Road, 169#, 430000 Wuhan, China, e-mail:

This work was supported by the Natural Science Foundation of Hubei Province (2000J052) and the Dominant Discipline’s Leader Project of Wuhan (20065006131-02).

References

[1] Huang JM, Wang WJ, Li BG, Zhu SP. Macromol. Mater. Eng. 2013, 298, 391–399.Search in Google Scholar

[2] Nori A, Kopecek J. Adv. Drug Deliv. Rev. 2005, 57, 609–636.Search in Google Scholar

[3] Ouimet MA, Griffin J, Carbone-Howell AL, Wu WH, Stebbins ND, Di R, Uhrich KE. Biomacromolecules 2013, 14, 854–861.10.1021/bm3018998Search in Google Scholar

[4] Kim SH, Kim JW, Kim DH, Han SH, Weitz DA. Small 2013, 9, 124–131.10.1002/smll.201201709Search in Google Scholar

[5] EI-Husseiny M, Patel S, Macfarlane RJ, Haddad FS. J. Bone Joint Surg. Br. 2011, 93, 151–157.Search in Google Scholar

[6] Mendel V, Simanowski HJ, Scholz HC, Heymann H. Arch. Orthop. Trauma. Surg. 2005, 125, 363–368.Search in Google Scholar

[7] Kanellakopoulou K, Giamarellos-Bourboulis EJ. Drugs 2000, 59, 1223–1232.10.2165/00003495-200059060-00003Search in Google Scholar

[8] Cui L, Cohen JL, Chu CK, Wich PR, Kierstead PH, Frechet JMJ. J. Am. Chem. Soc. 2012, 134, 15840–15848.Search in Google Scholar

[9] Tao CA, Wang JF, Qin SQ, Lv YA, Long Y, Jiang ZH. J. Mater. Chem. 2012, 22, 24856–24861.Search in Google Scholar

[10] Zhang SD, Tao QH, Wang ZY, Zhang QP. J. Mater. Chem. 2012, 22, 20166–20169.Search in Google Scholar

[11] Muthumanickkam A, Elankavi E, Gayathri R, Sampathkumar SK, Vijayakumar G, Muthukumar K, Subramanian S. Int. J. Mat. Res. 2010, 12, 1548–1553.Search in Google Scholar

[12] Sahoo D, Nayak PL. Int. J. Mat. Res. 2012, 11, 1395–1399.Search in Google Scholar

[13] Zhao HB, Cui ZX, Sun XF, Turng S, Peng XF. Ind. Eng. Chem. Res. 2013, 52, 2569–2581.Search in Google Scholar

[14] Ray SS, Okamoto M. Prog. Polym. Sci. 2003, 28, 1539–1641.Search in Google Scholar

[15] Kathryn EU. Chem. Rev. 1999, 99, 3181–3198.Search in Google Scholar

[16] Domb AJ, Langer RS. J. Polym. Sci., Part A: Polym. Chem. 1987, 25, 3373–3386.Search in Google Scholar

[17] Chen LB, Wang H, Shang L. J. Biomed. Mater. Res. Part B: Appl. Biomater. 2007, 83, 589–595.Search in Google Scholar

[18] Gao J, Bao F, Feng LL, Shen KY, Zhu QD, Wang DF, Chen T, Ma R, Yan CJ. RSC Advances 2011, 1, 1737–1744.10.1039/c1ra00029bSearch in Google Scholar

[19] Wu CS, Liao HT. Polymer 2007, 48, 4449–4458.10.1016/j.polymer.2007.06.004Search in Google Scholar

[20] Islam MS, Pickering KL, Foreman NJ. J. Polym. Environ. 2010, 18, 696–704.Search in Google Scholar

[21] Gong K, Rehman IU, Darr JA. Int. J. Pharm. 2007, 338, 191–197.Search in Google Scholar

[22] Day M, Victoria A, Liao X. J. Therm. Anal. Calorim. 2006, 86, 623–629.Search in Google Scholar

[23] Mathiowitz E, Amato C, Dor P, Langer R. Polymer 1990, 31, 547–555.10.1016/0032-3861(90)90401-JSearch in Google Scholar

[24] Le CP, Estebe JP, Clement R, Du PL, Chevanne F, Ecoffey C, Le VR. Int. J. Pharm. 2002, 238, 191–203.Search in Google Scholar

[25] Tisserat B, Finkenstadt. J. Polym. Environ. 2011, 19, 766–775.Search in Google Scholar

[26] EI-Newehy MH, Elsherbiny AS, Mori H. J. Appl. Polym. Sci. 2013, 127, 4918–4926.Search in Google Scholar

Received: 2013-3-22
Accepted: 2013-8-5
Published Online: 2013-08-30
Published in Print: 2013-10-01

©2013 by Walter de Gruyter Berlin Boston

Downloaded on 3.12.2025 from https://www.degruyterbrill.com/document/doi/10.1515/polyeng-2013-0071/html
Scroll to top button