Search Results

You are looking at 1 - 10 of 794 items for :

  • Refine by Access: All Content x
Clear All

, HPTLC: Quantitative Analysis of Pharmaceutical Formulations, CBS, New Delhi, 1996, pp. 162–165. Sethi P.D. HPTLC: Quantitative Analysis of Pharmaceutical

Restricted access

16 45 47 P.D. Sethi , HPTLC: Quantitative Analysis of Pharmaceutical Formulations, CBS, New Delhi, 1996, pp. 162

Restricted access

. P.D. Sethi , HPTLC: High Performance Thin-layer Chromatography; Quantitative Analysis of Pharmaceutical Formulations, CBS Publishers & Distributors, New Delhi, 1996. Sethi P

Restricted access

.G. Nayak, B.M. Mohan , International Symposium for Thin Layer Chromatography HPTLC 2006, Berlin, 9–11October 2006 (unpublished). M. Acikkol, S. Semen, Z. Turkmen, S. Mercan , J. Planar Chromatogr. 25

Restricted access

E. Reich and A. Blatter , HPTLC for the Analysis of Herbal drugs, Herbal Drug Preparations and Herbal Medicinal Products. In: J. Sherma and B. Fried (Eds) Handbook of Thin

Restricted access

). E. Reich , Qualitative and Quantitative Analysis of Herbals and Herbal Medicinal Products (HMP) by HPTLC. In: Sz. Nyiredy (Ed.) Proc. Int. Symp. Planar Separations — Planar Chromatography 2000, Lillafüred, pp. 45

Restricted access

otitis media, non-streptococcal bacterial pharyngitis. Literature survey indicated availability of stability-indicating high-performance liquid chromatography (HPLC) [ 3 – 23 ], high-performance thin-layer chromatography (HPTLC) [ 24 – 26 ], and

Open access
JPC - Journal of Planar Chromatography - Modern TLC
Authors:
Vijay Mirakor
,
Vikas Vaidya
,
Sasikumar Menon
,
Parikshit Champanerker
, and
Avdhoot Laud

An HPTLC method, using an internal standard, for analysis of colchicine in a pharmaceutical formulation, has been established and validated. The analyte and internal standard were separated on aluminum plates precoated with silica gel 60 F 254 ; the mobile phase was ethyl acetate-acetonitrile-water-formic acid 8.0:1.0:0.5:0.5 ( v/v ). Quantification was by densitometric scanning at 358 nm. Response was a linear function of colchicine concentration in the range 5 to 35 μg mL −1 . The limits of detection and quantification for colchicine were 1 and 5 μg mL −1 , respectively. Average recovery of colchicine was 100.48%, which showed the method was free from interference from excipients present in the formulation. The established method enabled accurate, precise, and rapid analysis of colchicine in the pharmaceutical formulation.

Restricted access

Residues of three pyrethroids in spiked vegetables have been analyzed by HPTLC with two mobile phases in a twin-trough chamber and in horizontal chambers. The spots were detected at λ = 203 nm and the greatest detection sensitivity for the three pyrethroids was 10 ng. Recovery after fortification at 0.5–5.0 mg kg −1 was from 70.20 to 108.5%. The relative standard deviation was 1.59–27.94%.

Restricted access

2001 Pulse 7 13 . [16]. P.D. Sethi 1996 HPTLC Quantitative

Full access