Malinovsky J M, Bernard J M, Le Corre P, Dumand J B, Lepage J Y, Le Verge R, Souron R
Département d'Anesthésie-Réanimation Chirurgicale, Hôtel-Dieu, Nantes, France.
Anesth Analg. 1995 Sep;81(3):519-24. doi: 10.1097/00000539-199509000-00016.
The incorporation of local anesthetics into injectable polymer microspheres can be useful in providing prolonged regional effects. This randomized study was designed to compare the effects of bupivacaine and bupivacaine-loaded microspheres on the time course of motor block in rabbits injected epidurally. Bupivacaine-loaded microspheres and drug-free microspheres 1-10 microns in size were devised from poly-d,l-lactic acid by using a solvent evaporation/extraction method. The effects of bupivacaine and of similar amounts of bupivacaine-loaded microspheres were studied in 26 rabbits as follows: 0.9% sodium chloride, followed by drug-free microspheres, then 1.25 mg of bupivacaine and 1.25 mg of bupivacaine-loaded microspheres (Group I; n = 8); 2.5 mg of bupivacaine, then 2.5 mg of bupivacaine-loaded microspheres (Group II; n = 8); and 5 mg of bupivacaine and 5 mg of bupivacaine-loaded microspheres (Group III; n = 10). Motor block was evaluated blindly by observation of walking disturbances, using a scale from 0 (free movements) to 3 (total limb paralysis). A period of 3 days elapsed between each injection. No limitation on movements was observed after 0.9% sodium chloride and drug-free microsphere injection. With 5 mg, both bupivacaine solutions provided complete motor block which was significantly more prolonged (+244% +/- 129%, mean +/- SD) with bupivacaine-loaded microspheres than bupivacaine. With 2.5 and 1.25 mg, block intensity was less marked, and block duration was shorter after administration of bupivacaine-loaded microspheres than after bupivacaine. We concluded that blocks resulting from bupivacaine-loaded microspheres are highly influenced by the amount of drug initially released by the polymer.
将局部麻醉剂加入可注射聚合物微球中,可能有助于产生持久的局部效应。这项随机研究旨在比较布比卡因和载有布比卡因的微球对硬膜外注射兔子运动阻滞时间过程的影响。通过溶剂蒸发/萃取法,由聚-d,l-乳酸制成了尺寸为1-10微米、载有布比卡因的微球和无药物微球。在26只兔子中研究了布比卡因和等量载有布比卡因的微球的效果,如下:0.9%氯化钠,接着是无药物微球,然后是1.25毫克布比卡因和1.25毫克载有布比卡因的微球(第一组;n = 8);2.5毫克布比卡因,然后是2.5毫克载有布比卡因的微球(第二组;n = 8);以及5毫克布比卡因和5毫克载有布比卡因的微球(第三组;n = 10)。通过观察行走障碍,采用从0(自由活动)到3(肢体完全麻痹)的量表,对运动阻滞进行盲法评估。每次注射之间间隔3天。注射0.9%氯化钠和无药物微球后未观察到运动受限。使用5毫克时,两种布比卡因溶液均产生了完全运动阻滞,载有布比卡因的微球产生的运动阻滞明显更持久(+244%±129%,平均值±标准差)。使用2.5毫克和1.25毫克时,阻滞强度较小,载有布比卡因的微球给药后阻滞持续时间比布比卡因给药后短。我们得出结论,载有布比卡因的微球产生的阻滞受聚合物最初释放的药物量的高度影响。