Degradable poly(anhydride ester) implants: effects of localized salicylic acid release on bone

被引:85
作者
Erdmann, L
Macedo, B
Uhrich, KE
机构
[1] Rutgers State Univ, Dept Chem, Piscataway, NJ 08854 USA
[2] Univ Med & Dent New Jersey, New Jersey Med Sch, Ctr Dent & Oral Hlth, Newark, NJ 07103 USA
关键词
poly(anhydride ester); salicylic acid; degradable; bone formation; bone resorption;
D O I
10.1016/S0142-9612(00)00118-6
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Degradable poly(anhydride ester) implants in which the polymer backbone breaks down into salicylic acid (SA) were investigated. In this preliminary work, local release of SA from the poly(anhydride esters), thus classified as 'active polymers', on healthy bone and tissue was evaluated in vivo using a mouse model. Degradable polyanhydrides that break down into inactive by-products were used as control membranes because of their chemical similarity to the active polymers. Small polymer squares were inserted over the exposed palatal bone adjacent to the maxillary first molars. Active polymer membranes were placed on one side of the mouth, control polymers placed on the contralateral side. Intraoral clinical examination showed that active polymer sites were less swollen and inflamed than control polymer sites. Histopathological examination at day 1 showed essentially no difference between control and active polymers. After 4 days, active polymer sites showed epithelial proliferation to a greater extent than the polyanhydride controls. After 20 days, active polymer sites showed greater thickness of new palatal bone and no resorptive areas, while control polymer sites showed less bone thickness as well as resorption including lacunae involving cementum and dentine. From these preliminary studies, we conclude that active polymers, namely poly(anhydride esters), stimulated new bone formation. (C) 2000 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:2507 / 2512
页数:6
相关论文
共 21 条
[1]   INTERSTITIAL CHEMOTHERAPY WITH DRUG POLYMER IMPLANTS FOR THE TREATMENT OF RECURRENT GLIOMAS [J].
BREM, H ;
MAHALEY, S ;
VICK, NA ;
BLACK, KL ;
SCHOLD, SC ;
BURGER, PC ;
FRIEDMAN, AH ;
CIRIC, IS ;
ELLER, TW ;
COZZENS, JW ;
KENEALY, JN .
JOURNAL OF NEUROSURGERY, 1991, 74 (03) :441-446
[2]   PLACEBO-CONTROLLED TRIAL OF SAFETY AND EFFICACY OF INTRAOPERATIVE CONTROLLED DELIVERY BY BIODEGRADABLE POLYMERS OF CHEMOTHERAPY FOR RECURRENT GLIOMAS [J].
BREM, H ;
PIANTADOSI, S ;
BURGER, PC ;
WALKER, M ;
SELKER, R ;
VICK, NA ;
BLACK, K ;
SISTI, M ;
BREM, S ;
MOHR, G ;
MULLER, P ;
MORAWETZ, R ;
SCHOLD, SC .
LANCET, 1995, 345 (8956) :1008-1012
[3]   SOLUBLE FUNCTIONAL POLYMERS .3. A POLYMERIC DRUG FOR TREATMENT OF INFLAMMATORY BOWEL-DISEASE [J].
BROWN, JP ;
MCGARRAUGH, GV ;
PARKINSON, TM ;
WINGARD, RE ;
ONDERDONK, AB .
JOURNAL OF MEDICINAL CHEMISTRY, 1983, 26 (09) :1300-1307
[4]   Polyanhydrides: the effects of ring substitution changes on polymer properties [J].
Campo, CJ ;
Anastasiou, T ;
Uhrich, KE .
POLYMER BULLETIN, 1999, 42 (01) :61-68
[5]   Synthesis and degradation characteristics of salicylic acid-derived poly(anhydride-esters) [J].
Erdmann, L ;
Uhrich, KE .
BIOMATERIALS, 2000, 21 (19) :1941-1946
[6]  
ERDMANN L, 1998, ACS SYM SER, P83
[7]   USE OF DIGITAL RADIOGRAPHY TO DEMONSTRATE THE POTENTIAL OF NAPROXEN AS AN ADJUNCT IN THE TREATMENT OF RAPIDLY PROGRESSIVE PERIODONTITIS [J].
JEFFCOAT, MK ;
PAGE, R ;
REDDY, M ;
WANNAWISUTE, A ;
WAITE, P ;
PALCANIS, K ;
COGEN, R ;
WILLIAMS, RC ;
BASCH, C .
JOURNAL OF PERIODONTAL RESEARCH, 1991, 26 (05) :415-421
[8]  
KORMAN K, 1990, J PERIODONTAL RES, V25, P300
[9]  
Kubo K, 1998, J BIOMED MATER RES, V39, P554, DOI 10.1002/(SICI)1097-4636(19980315)39:4<554::AID-JBM8>3.0.CO
[10]  
2-I