Pharmacological and Pharmacokinetic Studies with Vitamin D-loaded Nanoemulsions in Asthma Model.
Inflammation. 2013 Dec 11.
Wei-Hong T, Min-Chang G, Zhen X, Jie S. sunjiehuzhou at yeah.net
Taizhou Enze Medical Center Zhejiang Hospital, Zhejiang, 318050, People's Republic of China.
Vitamin D (VD) was studied for its anti-inflammatory activities with prepared VD-loaded nanoemulsions (VDNM) in ovalbumin-induced asthmatic mice in this paper.
In this study, we prepared VDNM for the delivery of VD from the established composition of solid self-emulsifying drug delivery systems (sSEDDS) by spray-drying technique and evaluated its bioavailability (BA) and anti-inflammatory activities in experimental allergic asthma. After the mice were treated orally with VD or VDNM, the plasma 25(OH) D levels, polymorphonuclear cells, tumor necrosis factor alpha (TNF-α), interleukin 1 beta (IL-1β), total antioxidant activity, and C3 and C4 complement protein levels were studied, respectively.
Treatment with VDNM reduced
- MPO activity,
- oxidative stress,
- C3 protein level,
- O2 - level as well as the
- production of IL-1β and TNF-α.
Pharmacokinetic studies showed that a significant increase in the maximum concentration (C max) and AUC0→24 h were observed in VDNM group when compared with VD group (P < 0.01).
The result revealed that VDNM led to an improvement in oral BA of VD in a murine ovalbumin-induced asthma model. These data provided an important proof that VDNM might be a new potential therapy for the management of asthma in humans.
PMID: 24326945
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Note:
- The nanoemulsion had a better bioavailability than standard oral vitamin D.
- It does not indicate how much better: 2%. 20%, 200%?
- It does not indicate if it actually helped reduce asthma