Enhanced neuroprotective and antidepressant activity of curcumin-loaded nanostructured lipid carriers in lipopolysaccharide-induced depression and anxiety rat model

被引:51
|
作者
Rubab, Sana [1 ]
Naeem, Komal [1 ]
Rana, Isra [1 ]
Khan, Namrah [1 ]
Afridi, Maryam [2 ]
Ullah, Izhar [3 ]
Shah, Fawad Ali [1 ]
Sarwar, Sadia [1 ]
Din, Fakhar Ud [4 ]
Choi, Ho-Ik [5 ]
Lee, Cheol-Ho [5 ]
Lim, Chang-Wan [5 ]
Alamro, Abir Abdullah [6 ]
Kim, Jin-Ki [5 ]
Zeb, Alam [1 ]
机构
[1] Riphah Int Univ, Riphah Inst Pharmaceut Sci, Sect G-7-4,7th Ave, Islamabad 44000, Pakistan
[2] Kohat Univ Sci & Technol, Dept Pharm, Kohat, Pakistan
[3] Univ Poonch, Fac Med & Hlth Sci, Dept Pharm, Rawalakot, Ajk, Pakistan
[4] Quaid I Azam Univ, Dept Pharm, Islamabad, Pakistan
[5] Hanyang Univ, Coll Pharm, Inst Pharmaceut Sci & Technol, 55 Hanyangdaehak Ro, Ansan 44000, Gyeonggi, South Korea
[6] King Saud Univ, Coll Sci, Dept Biochem, Riyadh, Saudi Arabia
基金
新加坡国家研究基金会;
关键词
Curcumin; Nanostructured lipid carriers; Antidepressant activity; Anxiolytic activity; Neuroprotection; Neuroinflammation; BLOOD-BRAIN-BARRIER; DRUG-DELIVERY SYSTEMS; FORCED SWIM TEST; IN-VITRO; NANOPARTICLES; BIOAVAILABILITY; DESIGN; INFLAMMATION; BEHAVIOR; NEUROINFLAMMATION;
D O I
10.1016/j.ijpharm.2021.120670
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The present study aims to develop curcumin-loaded nanostructured lipid carriers (CUR-NLCs) and investigate their neuroprotective effects in lipopolysaccharide (LPS)-induced depression and anxiety model. Nanotemplate engineering technique was used to prepare CUR-NLCs with Compritol 888 ATO and oleic acid as solid and liquid lipid, respectively. Poloxamer 188, Tween 80 and Span 80 were used as stabilizing agents for solid-liquid lipid core. The physicochemical parameters of CUR-NLCs were determined followed by in vitro drug release and in vivo neuroprotective activity in rats. The optimized CUR-NLCs demonstrated nanometric particle size of 147.8 nm, surface charge of -32.8 mV and incorporation efficiency of 91.0%. CUR-NLCs showed initial rapid followed by a sustained drug release reaching up to 73% after 24 h. CUR-NLCs significantly elevated struggling time and decreased immobility time in forced swim and tail suspension tests. A substantial increase in time spent and number of entries into the light and open compartments was observed in light-dark box and elevated plus maze models. CUR-NLCs improved the tissue architecture and suppressed the expression of p-NF-kappa B, TNF-alpha and COX-2 in brain tissues from histological and immunohistochemical analysis. CUR-NLCs improved the neuroprotective effect of curcumin and can be used as a potential therapeutics for depression and anxiety.
引用
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页数:13
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