Planta Med 2010; 76(5): 474-480
DOI: 10.1055/s-0029-1186219
Analytical Studies
Original Papers
© Georg Thieme Verlag KG Stuttgart · New York

HPTLC Densitometric Evaluation of Tissue Culture Extracts of Nothapodytes foetida Compared to Conventional Extracts for Camptothecin Content and Antimicrobial Activity

Ajay Gajanan Namdeo1 , Ajay Sharma1 , Lohidasan Sathiyanarayanan2 , Devanand Fulzele3 , Kakasaheb Ramoo Mahadik2
  • 1Department of Pharmacognosy, Poona College of Pharmacy, Bharati Vidyapeeth University, Pune, India
  • 2Department of Pharmaceutical Chemistry, Poona College of Pharmacy, Bharati Vidyapeeth University, Pune, India
  • 3Plant Biotechnology Division, Bhabha Atomic Research Centre, Trombay, Mumbai, India
Further Information

Publication History

received April 21, 2009 revised Sept. 9, 2009

accepted Sept. 14, 2009

Publication Date:
27 October 2009 (online)

Abstract

Tissue culture technique is becoming popular because of its well-known ability to enhance the content of secondary metabolites in plants. Callus tissue cultures of Nothapodytes foetida were developed using 250 different medium compositions to optimize this procedure. Methanolic extracts of callus (MEC) and of various parts of N. foetida were comparatively analyzed for camptothecin content, and a high performance thin layer chromatography method was developed for its quantitation. Chloroform-ethylacetate-methanol (4 : 5 : 0.5 v/v) was used as the mobile phase. The method was validated for linearity, precision (interday and intraday), repeatability, limit of detection (LOD), limit of quantitation (LOQ), and accuracy. The relationship between the concentration of standard solutions and the peak response was linear within the range of 80 to 480 ng/spot with a correlation coefficient of 0.998 ± 0.020. Instrumental precision was evaluated as 0.54 (% CV). Repeatability of sample and standard were estimated to be 1.08 and 1.01 (% CV), and LOD and LOQ were found to be 40 and 80 ng/spot, respectively. The accuracy of the method was checked out by a recovery study and the average percentage recovery was calculated as being 99.13 %. The methanolic extract of callus grown in tissue culture with medium composition picloram + thidiazuron + gibberellic acid (1 : 1 : 4; MEC‐PTG) showed a higher percentage of camptothecin (5.74 % w/v) than the methanolic extract of fruits (3.56 % w/w), leaves (1.56 % w/w), stem (1.19 % w/w), and root (1.11 % w/w). The results of the antimicrobial screening indicate that MEC‐PTG exhibited maximum activity against all microorganisms. Among the fungi tested, MEC‐PTG showed maximum activity against A. niger and C. albicans (MIC value 10 µg/mL) whereas among bacteria strains, its activity was highest against B. subtilis and S. lutea (MIC 20 µg/mL).

References

  • 1 Fu T J. Safety considerations for food ingredients produced by plant cell and tissue culture.  Chemtech. 1998;  28 40-46
  • 2 Antognoni F, Zheng S, Pagnucco C, Baraldi R, Poli F, Biondi S. Induction of flavonoid production by UV-B radiation in Passiflora quadrangularis callus cultures.  Fitoterapia. 2007;  78 345-352
  • 3 Fulzele D P, Satdive R K, Pol B B. Growth and production of camptothecin by cell suspension cultures of Nothapodytes foetida.  Planta Med. 2001;  67 150-152
  • 4 Wall M E, Wani M C. Camptothecin and analogs. From discovery to clinic. Boca Raton; CRC Press 1995: 21-41
  • 5 Priel E, Showalter S D, Blair D G. Inhibition of human immunodeficiency virus (HIV-l) replication in vitro by non-cytotoxic doses of camptothecin: a topoisomerase inhibitor.  Aids Res Human Retrovir. 1991;  7 65-72
  • 6 Takeuchi A, Dohashi K, Fujimoto S, Tanaka K, Suzuki M, Terashima Y, Hasumi K, Akiya K, Negishi Y, Tamaya T, Tanizawa O, Sugawa T, Umesaki T, Hashimoto M, Yajima A, Yakamizawa H, Sonoda T, Takada Y, Tomoda Y, Taguchi T. A late phase II study of CPT-II in uterine, cervical cancer and ovarian cancer.  Jpn J Cancer Chemother. 1991;  18 1661
  • 7 Potmesil M. Camptothecin from bench research to hospital.  Cancer Res. 1994;  54 1431-1439
  • 8 Bodley A F, Cumming J N, Shapiro T A. Effect of camptothecin, a topoisomerase I inhibitor, on Plasmodium falciparum.  Biochem Pharmacol. 1998;  55 709-711
  • 9 Gunasekera S P, Badawi M M, Cordell G A, Farnsworth N R. Plant anticancer agents X. Isolation of camptothecin and 9-methoxycamptothecin from Ervatamia heyneana.  J Nat Prod. 1979;  42 475-477
  • 10 Tafur S, Nelson J D, Delong D C, Svoboda G H. Antiviral components of Ophirrohiza mungos. Isolation of camptothecin and 10-methoxycamptothecin.  Lloydia. 1976;  39 261-262
  • 11 Saito K, Sudo H, Yamazaki M, Nakamura M, Kitajima M, Takayama H, Aimi N. Feasible production of camptothecin by hairy root culture of Ophiorrhiza pumila.  Plant Cell Rep. 2001;  20 267-271
  • 12 Fulzele D P, Satdive R K, Pol B B. Untransformed root cultures of Nothapodytes foetida and production of camptothecin.  Plant Cell Tissue Organ Cult. 2002;  69 285-288
  • 13 Sundravelan, Desireddy R B, Ciddi V. Camptothecin – a novel anticancer agent from tissue cultures of Nothapodytes foetida.  Indian J Pharm Sci. 2003;  65 101-105
  • 14 Dhalwal K, Biradar Y S, Rajani M. TLC densitometric method for simultaneous quantitation of phyllanthin, hypophyllanthin, gallic acid and ellagic acid in Phyllanthus amarus using HPTLC.  JAOAC Int. 2006;  89 619-623
  • 15 Ravishankara M N, Srivastava N, Jayathirtha M G, Padh H, Rajani M. Sensitive high performance thin layer chromatographic method for the estimation of diospyrin, a tumor inhibitory agent from the stem bark of Diospyros montana Roxb.  J Chromatogr B. 2000;  744 257-262
  • 16 Ravishankara M N, Srivastava N, Padh H, Rajani M. HPTLC method for the estimation of alkaloids of Cinchona officinalis stems bark and its marketed formulations.  Planta Med. 2001;  67 294-296
  • 17 Vuorela P, Rahko E L, Hiltunen R, Vuorela H. Extraction and planar chromatographic separation techniques in the separation of natural products.  J Chromatogr A. 1994;  670 191-198
  • 18 Fodor F K, Vigh Z, Turak N A, Renger B, Zeller M. Validation of high performance thin layer chromatographic methods for the identification of botanicals in a cGMP environment.  J AOAC Int. 2001;  84 1265-1276
  • 19 Doner L W. Determining sugar composition of food gum polysaccharides by HPTLC.  Chromatographia. 2001;  53 579-583
  • 20 WHO .Guidelines for the assessment of herbal medicine. Munich; World Health Organization 1991
  • 21 ICH .Q2A Validation of analytical procedure: methodology. Geneva; International Conference on Harmonization 1994
  • 22 ICH .Q2B Validation of analytical procedure: methodology. Geneva; International Conference on Harmonization 1996
  • 23 ICH .Guidance on analytical method validation. Toronto; International Convention on Quality for the Pharmaceutical Industry 2002
  • 24 Smania A, Delle M F, Smania E F A, Cuneo R S. Antibacterial activity of steroidal compounds isolated from Ganoderma applanatum fruit body.  Int J Med Mushrooms. 1999;  1 325-330
  • 25 Thengane S R, Kulkarni D K, Shrikhande V A, Joshi S P, Sonawane K B, Krishnamurthy K V. Influence of medium composition on callus induction and camptothecin(s) accumulation in Nothapodytes foetida.  Plant Cell Tissue Organ Cult. 2003;  72 247-251
  • 26 Roja G, Heble M R. The quinoline alkaloids camptothecin and 9-methoxycamptothecin from tissue cultures and mature trees of Nothapodytes nimmoniana.  Phytochemistry. 1994;  36 65-66
  • 27 Ciddi V, Shuler M L. Camptothecin from callus cultures of Nothapodytes foetida.  Biotechnol Lett. 2000;  22 129-132
  • 28 Dossantos L B O, Masini J C. Determination of picloram in natural watersemploying sequential injection square wave voltammetry using the hanging mercury drop electrode.  Talanta. 2007;  72 1023-1029
  • 29 Mcsteen P, Zhao Y. Plant hormones and signaling: common themes and new developments.  Dev Cell. 2008;  14 467-473
  • 30 Halvey A H, Mayak S. Interrelationship of several plant hormones in the regulation of rose petal senescences.  Acta Hort. 1975;  41 103-116
  • 31 Thimann K V. Plant senescence: a proposed integration of constituents processes.  Proc Ann Symp Plant Physiol. 1987;  10 1-19

Dr. Ajay G. Namdeo

Department of Pharmacognosy
Poona College of Pharmacy
Bharati Vidyapeeth University

Paud Road, Erandwane

411038 Pune, Maharashtra

India

Email: ajay_namdeo@rediffmail.com

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