Original ArticlePharmacognosy MagazineVol. 8 | Issue 30 | 2012 | pp. 129–134Open access
Biodistribution properties of cleistanthin A and cleistanthin B using magnetic resonance imaging in a normal and tumoric animal model
- 1*,
- 1,
- 2,
- 3,
- 2,
- 2,
- 2,
- 3,
- 4
- 1 Departments of Pharmacology, Institute of Postgraduate Medical Education and Research, Pondicherry, India.
- 2 Nanobiotechnology and Hepatitis B/AIDs, Pasteur Institute of Iran, Tehran, Iran.
- 3 Radiodiagnosis and.
- 4 Nuclear Medicine, Jawaharlal Institute of Postgraduate Medical Education and Research, Pondicherry, India.
Published in Pharmacognosy Magazine
Correspondence: Subramani Parasuraman
Departments of Pharmacology, Institute of Postgraduate Medical Education and Research, Pondicherry, India.
Copyright: © 2012 Manuscript Technomedia. This is an open access article.
- Published:
- May 23, 2012
- Received:
- Aug 23, 2011
How to cite
Parasuraman, S., Raveendran, R., Ardestani, M. S., Ramesh, A., Jabbari-Arabzadeh, A., Alavidjeh, M. S., Aghasadeghi, M. R., Elangovan, S., & Dhanapathi, H. (2012). Biodistribution properties of cleistanthin A and cleistanthin B using magnetic resonance imaging in a normal and tumoric animal model. Pharmacognosy Magazine, 8(30), 129–134. https://doi.org/10.4103/0973-1296.96559
Abstract
Aim: To determine the biodistribution properties of cleistanthin A and cleistanthin B in rodents using magnetic resonance imaging (MRI). Materials and Methods: Cleistanthins A and B, constituents of Cleistanthus collinus Roxb., were labelled with gadolinium (Gd3+) 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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Article metadata
| Title | Biodistribution properties of cleistanthin A and cleistanthin B using magnetic resonance imaging in a normal and tumoric animal model |
|---|---|
| Authors | Subramani Parasuraman; Ramasamy Raveendran; Mehdi Shafiee Ardestani; Ananthakrishnan Ramesh; Ali Jabbari-Arabzadeh; Mohammad Shafiee Alavidjeh; Mohammad Reza Aghasadeghi; Sundararajan Elangovan; Halanaik Dhanapathi |
| Affiliations | Departments of Pharmacology, Institute of Postgraduate Medical Education and Research, Pondicherry, India.; Nanobiotechnology and Hepatitis B/AIDs, Pasteur Institute of Iran, Tehran, Iran.; Radiodiagnosis and.; Nuclear Medicine, Jawaharlal Institute of Postgraduate Medical Education and Research, Pondicherry, India. |
| Journal | Pharmacognosy Magazine |
| Volume / Issue | Vol. 8, Issue 30 (2012) |
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