�?�Real-Time Oral Biodistribution of Fluorescent Labelle | 50095
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International Research Journal of Pharmacy and Pharmacology

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�?�Real-Time Oral Biodistribution of Fluorescent Labelled Olmesartan Medoxomil SMEDDS


Yelda Komesli

Statement of the Problem: Nowadays, the use of fluorescent labeled molecules with near infrared (NIR) dye at in vivo imaging, are increasingly common in the pharmaceutical field. Several studies were conducted using in vivo imaging technique to determine the biological characteristics, biodistribution and toxicity of different drug carriers like microbubbles [1], nanobubbles, nanocapsules, nanodevices, polymer-shelled agents and nanoparticles [2]. Although there were many studies on the imaging of the drugs after iv injection, there have been no oral biodistribution studies similar to our study. BCS Clas II type, antihypertensive drug Olmesartan Medoxomil (OM) is a prodrug which is converted to olmesartan with low bioavailability in the gastrointestinal tract. The aim of this work was to prove increased oral biodistribution of Olmesartan by fluorescent labelled Self-Microemulsifying Drug Delivery System (SMEDDS). In this study, VivoTag® 680 XL was chosen for the determination of the biodistribution of OM-SMEDDS because SMEDDS includes nano and microsize of droplets and small molecules. The second dye, lipophilic infrared fluorescent cyanine Xenolight® DiR was selected due to the lipid characteristics of SMEDDS. Labelled OM-SMEDDS and control dye administered group of mice visualised and emission values were recorded during the experiment [3]. Preparation of OM-SMEDDS: The experiments were carried out using our previous standardized and optimized SMEDDS and validated HPLC method that reported in our previous article [4]. The precipitated OM-SMEDDS was transferred to another epandorf  and the remaining washed portion was administered with 150 μl of oral gavage to the mice [3]. Findings: The fluorescent efficiency was calculated with Living Image® 4.4 software. Because the stomach has a dominant luminescence, the measurements were made with and without stomach. Representing the real-time biodistribution of OM-SMEDDS in vivo region of interest (ROI) values and ex vivo findings were recorded at predetermined times. (Figure 1). The results were statistically evaluated with one-way ANOVA (Analysis of variance) method. Differences in p values were considered significant (p<0.05). Conclusion & Significance: In this present study, a biocompatible imaging technique that can pass through the gastrointestinal tract has been developed for the first time. Real-time in vivo imaging of oral biodistribution of fluorescence labeled OM-SMEDSS was performed successfully.

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