Thyrotropin-Releasing Hormone Loaded and Chitosan Engineered Polymeric Nanoparticles: Towards Effective Delivery of Neuropeptides

被引:8
作者
Kaur, Sarabjit [1 ,2 ]
Bhararia, Avani [1 ,2 ]
Sharna, Krishna K. [3 ]
Mittal, Sherry [1 ,2 ]
Jain, Rahul [3 ]
Wangoo, Nishima [4 ]
Sharma, Rohit K. [1 ,2 ]
机构
[1] Panjab Univ, Dept Chem, Sect 14, Chandigarh 160014, India
[2] Panjab Univ, Ctr Adv Studies Chem, Sect 14, Chandigarh 160014, India
[3] NIPER, Dept Med Chem, Sect 67, Mohali 160062, Punjab, India
[4] Panjab Univ, Univ Inst Engn & Technol, Dept Appl Sci, Sect 25, Chandigarh 160014, India
关键词
Polymeric Nanoparticles; Thyrotropin-Releasing Hormone; Poly(lactide-co-glycolide) PLGA; Chitosan; Neuropeptides; Nanoformulation; PLGA NANOPARTICLES; TRH ANALOGS; DRUGS; MECHANISMS; EPILEPSY; SOLVENT;
D O I
10.1166/jnn.2016.12431
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Thyrotropin-Releasing Hormone (TRH), a tripeptide amide with molecular formula L-pGlu-L-His-L-Pro-NH2, is used in the treatment of brain/spinal injury and certain central nervous system (CNS) disorders, including schizophrenia, Alzheimer's disease, epilepsy, depression, shock and ischemia due to its profound effects on the CNS. However, TRH's therapeutic activity is severely hampered because of instability and hydrophilicity owing to its peptidic nature which results into ineffective penetration into the blood brain barrier. In the present study, we report the synthesis and stability studies of novel chitosan engineered TRH encapsulated poly(lactide-co-glycolide) (PLGA) based nanoformulation. The aim of such an encapsulation is to allow effective delivery of TRH in biological systems as the peptidase degrade naked TRH. The synthesis of TRH was carried out manually in solution phase followed by its encapsulation using PLGA to form polymeric nanoparticles (NPs) via nanoprecipitation technique. Different parameters such as type of organic phase, concentration of stabilizer, ratio of organic phase and aqueous phase, rate of addition of organic phase were optimized, tested and evaluated for particle size, encapsulation efficiency, and stability of NPs. The TRH-PLGA NPs were then surface modified with chitosan to achieve positive surface charge rendering them potential membrane penetrating agents. PLGA, PLGA-TRH, Chitosan-PLGA and Chitosan-PLGA-TRH NPs were characterized and analyzed using Dynamic Light Scattering (DLS), Transmissiom Electron Microscopy (TEM) and Infra-red spectroscopic techniques.
引用
收藏
页码:5324 / 5332
页数:9
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