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Bergenin determination in different extracts by high-performance thin-layer chromatographic densitometry
Masood Shah Khan1, Washim Khan1, Wasim Ahmad1
1Department of Pharmacognosy and Phytochemistry, Bioactive Natural Product Laboratory, Faculty of Pharmacy, Hamdard University, Hamdard Nagar, New Delhi, India.
A new high-performance thin-layer chromatographic (HPTLC) method quantifies bergenin in the medicinal plant Bergenia ligulata. This HPTLC method ensures the quality control of herbal medicines and detects adulterants.
Area of Science:
- Phytochemistry
- Analytical Chemistry
- Pharmacognosy
Background:
- Bergenia ligulata (Pashanbhed) is a medicinal plant used for kidney and liver disorders.
- Its rhizome is often adulterated, necessitating quality control measures.
- Bergenin is the key active metabolite in B. ligulata.
Purpose of the Study:
- To develop a High-Performance Thin-Layer Chromatographic (HPTLC) method for quantifying bergenin.
- To ensure the quality control of Bergenia ligulata and its traditional formulations.
- To detect adulterants in herbal products.
Main Methods:
- A sensitive HPTLC method was developed using precoated silica gel plates.
- Chloroform: methanol: acetic acid (8:1:1, v/v/v) served as the mobile phase.
- Quantification was performed by densitometry at 276 nm.
Main Results:
- The retention factor (Rf) of bergenin was 0.28 ± 0.03.
- Linearity was confirmed in the range of 200-5000 ng (r² = 0.999).
- Bergenin content was 5.51 ± 0.14% in methanolic extract and 5.76 ± 0.16% in acetone extract.
Conclusions:
- The developed HPTLC method is suitable for quality control and standardization.
- This method can effectively identify adulterants in B. ligulata and its formulations.
- Ensures the authenticity and therapeutic efficacy of herbal medicines.
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