Meunier J-P, Cardot J-M, Manzanilla E G, Wysshaar M, Alric M
Equipe de Recherche Technologique, Conception, Ingénierie et Développement de l'Aliment et du Médicament, Centre de Recherche en Nutrition Humaine, Faculté de Pharmacie, Université d'Auvergne, Clermont-Ferrand, France.
J Anim Sci. 2007 Oct;85(10):2699-710. doi: 10.2527/jas.2007-0027. Epub 2007 Apr 27.
The aim of this study was to develop sustained release microspheres of capsicum oleoresin as an alternative to in-feed additives. Two spray-cooling technologies, a fluidized air bed using a spray nozzle system and a vibrating nozzle system placed on top of a cooling tower, were used to microencapsulate 20% of capsicum oleoresin in a hydrogenated, rapeseed oil matrix. Microencapsulation was intended to reduce the irritating effect of capsicum oleoresin and to control its release kinetics during consumption by the animal. Particles produced by the fluidized air bed process (batch F1) ranged from 180 to 1,000 microm in size. The impact of particle size on release of capsaicin, the main active compound of capsicum oleoresin, was studied after sieving batch F1 to obtain 4 formulations: F1a (180 to 250 microm), F1b (250 to 500 microm), F1c (500 to 710 microm), and F1d (710 to 1,000 microm). The vibrating nozzle system can produce a monodispersive particle size distribution. In this study, particles of 500 to 710 microm were made (batch F2). The release kinetics of the formulations was estimated in a flow-through cell dissolution apparatus (CFC). The time to achieve a 90% dissolution value (T90%) of capsaicin for subbatches of F1 increased with the increase in particle size (P < 0.05), with the greatest value of 165.5 +/- 13.2 min for F1d. The kinetics of dissolution of F2 was slower than all F1 subbatches, with a T90% of 422.7 +/- 30.0 min. Nevertheless, because CFC systems are ill suited for experiments with solid feed and thus limit their predictive values, follow-up studies were performed on F1c and F2 using an in vitro dynamic model that simulated more closely the digestive environment. For both formulations a lower quantity of capsaicin dialyzed was recorded under fed condition vs. fasting condition with 46.9% +/- 1.0 vs. 74.7% +/- 2.7 for F1c and 32.4% +/- 1.4 vs. 44.2% +/- 2.6 for F2, respectively. This suggests a possible interaction between capsaicin and the feed matrix. Moreover, 40.4 +/- 3.9% of the total capsaicin intake in F2 form was dialyzed after 8 h of digestion when feed had been granulated vs. 32.4 +/- 1.4% when feed had not been granulated, which suggests that the feed granulation process could lead to a partial degradation of the microspheres and to a limitation of the sustained release effect. This study demonstrates the potential and the limitations of spray-cooling technology to encapsulate feed additives.
本研究的目的是开发辣椒油树脂缓释微球,作为饲料添加剂的替代品。采用两种喷雾冷却技术,即使用喷嘴系统的流化床和气冷塔顶部的振动喷嘴系统,将20%的辣椒油树脂微囊化于氢化菜籽油基质中。微囊化旨在降低辣椒油树脂的刺激作用,并控制其在动物食用期间的释放动力学。流化床工艺(批次F1)生产的颗粒尺寸范围为180至1000微米。对批次F1进行筛分以获得4种制剂:F1a(180至250微米)、F1b(250至500微米)、F1c(500至710微米)和F1d(710至1000微米),研究了粒径对辣椒油树脂主要活性成分辣椒素释放的影响。振动喷嘴系统可产生单分散的粒径分布。在本研究中,制备了500至710微米的颗粒(批次F2)。在流通池溶解装置(CFC)中评估制剂的释放动力学。F1子批次中辣椒素达到90%溶解值(T90%)的时间随粒径增加而增加(P<0.05),F1d的最大值为165.5±13.2分钟。F2的溶解动力学比所有F1子批次都慢,T90%为422.7±30.0分钟。然而,由于CFC系统不太适合固体饲料实验,因此限制了其预测价值,随后使用更接近模拟消化环境的体外动态模型对F1c和F2进行了后续研究。对于两种制剂,在喂食条件下与禁食条件下相比,透析出的辣椒素量较低,F1c分别为46.9%±1.0%与74.7%±2.7%,F2分别为32.4%±1.4%与44.2%±2.6%。这表明辣椒素与饲料基质之间可能存在相互作用。此外,当饲料制成颗粒时,F2形式的总辣椒素摄入量在消化8小时后有40.4±3.9%被透析,而未制成颗粒时为32.4±1.4%,这表明饲料制粒过程可能导致微球部分降解并限制缓释效果。本研究证明了喷雾冷却技术在包封饲料添加剂方面的潜力和局限性。