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Pharmacognosy Magazine 2012-Apr

Biodistribution properties of cleistanthin A and cleistanthin B using magnetic resonance imaging in a normal and tumoric animal model.

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Subramani Parasuraman
Ramasamy Raveendran
Mehdi Shafiee Ardestani
Ramesh Ananthakrishnan
Ali Jabbari-Arabzadeh
Mohammad Shafiee Alavidjeh
Mohammad Reza Aghasadeghi
Sundararajan Elangovan
Halanaik Dhanapathi

Palabras clave

Abstracto

OBJECTIVE

To determine the biodistribution properties of cleistanthin A and cleistanthin B in rodents using magnetic resonance imaging (MRI).

METHODS

Cleistanthins A and B, constituents of Cleistanthus collinus Roxb., were labelled with gadolinium (Gd(3+)) directly and injected into normal and tumoric nude mice. The tissue signal intensity was measured using MRI to perform a noninvasive kinetic assay. Wistar rats were used for determination of the grayscale intensity to observe the distribution patterns of of cleistanthins A and B.

RESULTS

Cleistanthin A is kinetically more attractive to the gastrointestinal tract than is cleistanthin B, which gets accumulated in muscular tissues of mice in greater concentrations compared with cleistanthin A. Cleistanthin B but not cleistanthin A showed tumoric affinity and exhibited a tumor kinetic attraction in tumoric mice. In rats, cleistanthin A showed greater grayscale intensities in the brain, liver, and skeletal muscles in immediate post contrast MRI images, whereas the gadolinium tagged cleistanthin B showed higher grayscale intensities in the cardiac muscle and skeletal muscles in delayed post contrast MRI images.

CONCLUSIONS

Cleistanthin A is more pharmacokinetically attractive to the gastrointestinal tract than cleistanthin B.

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