Al-Habdan Ibrahim, Sadat-Ali Mir, Safar Alghamdy Mastour, Randhawa Akram, Chathoth Shahanas
Department of Orthopaedic Surgery, University of Dammam, Saudi Arabia;
Department of Pharmacology, University of Dammam, Saudi Arabia;
Int J Biomed Sci. 2014 Sep;10(3):167-71.
Sadat-Habdan Mesenchymal Stimulating Peptide (SHMSP) was discovered and patented with USPTO in 2008. Studies have shown that SHMSP works as an angiogenesis factor. This study was done to evaluate pharmacokinetics (PK) in rats and toxicology studies in goats and rats.
In 80 skeletally mature Sprague Dawley rats 5 milligram/kg body weight of SHMSP was injected intramuscularly. Blood samples were collected at 0, 30, 60, 120, 240, 320 minutes and 480 minutes. The plasma calibration curves were prepared at concentrations of 6.25, 3.12, 1.56, 0.78 and 0.39 ng/mL by spiking 190 µL of rat plasma with 10µL of working standard and 200 µL of deionized water. Samples were vortexed for five seconds, centrifuged at 14000 rpm for 30 minutes at 4°C and the supernatant was collected analyzed using High-performance liquid chromatography (HPLC). After injection of 20 µL sample, the peptide was eluted with 15ml linear gradient up to 36% of eluent A. The time between injections was 25 min. and the eluent was monitored at a wavelength of 215 nm. The concentration of peptide present in the rat plasma samples collected at different time intervals were quantified using standard curve method. The goats were injected deep intramuscularly 100 mg/kg-body weight of the SHMSP dissolved in injection solution. In 10 Sprague Dawley rats of ≥250 grams of weight, 20 mg/kg/day SHMSP was injected for 7 consecutive days. All the animals were kept at a close watch. Clinical observation at least once daily and as necessary was undertaken. After 2 weeks animals were euthanized and major organs were harvested and histopathology samples were obtained and processed.
There were no deaths is either of the study and control group of animals. The gross observations of the various organs appeared normal and histopathological studies did not show any toxicity in the organs tested. The plasma concentration-time profile of SHMSP after intramuscular injection, the level of SHMSP in an initial high phase reaching the highest at 30 minutes 2.3184 ng/ml and 60 minutes 1.7447 ng/ml at 60 minutes. The lowest level was at 360 minutes of 0.0879 ng/ml.
The dose of SHMSP at 20 times the recommended dose was not toxic and secondly the peak time and level was at 30 minutes to 120 minutes and the plasma half-life of SHMSP was 90 minutes.
萨达特 - 哈布丹间充质刺激肽(SHMSP)于2008年被发现并获得美国专利商标局的专利。研究表明,SHMSP作为一种血管生成因子发挥作用。本研究旨在评估大鼠的药代动力学(PK)以及山羊和大鼠的毒理学研究。
在80只骨骼成熟的Sprague Dawley大鼠中,以5毫克/千克体重的剂量肌肉注射SHMSP。在0、30、60、120、240、320分钟和480分钟采集血样。通过向190微升大鼠血浆中加入10微升工作标准品和200微升去离子水,制备浓度为6.25、3.12、1.56、0.78和0.39纳克/毫升的血浆校准曲线。样品涡旋5秒,在4°C下以14000转/分钟离心30分钟,收集上清液并使用高效液相色谱(HPLC)进行分析。进样20微升样品后,肽用15毫升线性梯度洗脱,直至洗脱液A达到36%。进样间隔时间为25分钟,在215纳米波长下监测洗脱液。使用标准曲线法对在不同时间间隔采集的大鼠血浆样品中存在的肽浓度进行定量。将溶解在注射溶液中的SHMSP以100毫克/千克体重的剂量深部肌肉注射到山羊体内。在10只体重≥250克的Sprague Dawley大鼠中,连续7天每天注射20毫克/千克/天的SHMSP。对所有动物进行密切观察。每天至少进行一次临床观察,并根据需要进行观察。2周后对动物实施安乐死,摘取主要器官,获取并处理组织病理学样本。
研究组和对照组动物均无死亡。各器官的大体观察外观正常,组织病理学研究未显示所测试器官有任何毒性。肌肉注射后SHMSP的血浆浓度 - 时间曲线,SHMSP在初始高相水平在30分钟时达到最高,为2.3184纳克/毫升,60分钟时为1.7447纳克/毫升。最低水平在360分钟时,为0.0879纳克/毫升。
SHMSP剂量为推荐剂量的20倍时无毒,其次峰值时间和水平在30分钟至120分钟,SHMSP的血浆半衰期为90分钟。