Close
  Indian J Med Microbiol
 

Figure 5: (a) Representative histogram showing in vitro dose-dependent cytotoxicity of (A) aqueous extract of leaves, bark, and flowers on MCF-7 cells exposed for 24 h, (B) MCF-7 cells exposed to methanol extracts of plant parts exposed for 24 h, (C) MCF-7 cells exposed to ethanol extracts for 24 h, (D) MCF-7 cells exposed to aqueous extracts of plant parts exposed for 48 h, (E) MCF-7 cells exposed to methanol extracts of plant parts exposed for 48 h (F) MCF-7 cells exposed to ethanol extracts of plant parts exposed for 48 h. The results represent the means of three independent experiments, and error bars represent the standard error of the mean. (b) Cell morphology of MCF-7 cells after 48 h treatment of aqueous, methanol, and ethanol extracts of leaves, stem bark, and flowers of Lasiosiphon eriocephalus at different concentrations. All images are taken at ×20 magnification with Carl Zeiss phase contrast microscope. Scale bars, 100 μm. (c) Representative histogram showing in vitro dose dependent cytotoxicity of (A) aqueous extract of leaves, bark and flowers on HeLa cells exposed for 24 h, (B) HeLa cells exposed to methanol extracts of plant parts exposed for 24 h, (C) HeLa cells exposed to ethanol extracts for 24 h, (D) HeLa cells exposed to aqueous extracts of plant parts exposed for 48 h, (E) HeLa cells exposed to methanol extracts of plant parts exposed for 48 h (F) HeLa cells exposed to ethanol extracts of plant parts exposed for 48 h. The results represent the means of three independent experiments, and error bars represent the standard error of the mean. (d) Cell morphology of HeLacells after 48 h treatment of aqueous, methanol, and ethanol extracts of leaves, stem bark, and flowers of Lasiosiphon eriocephalus at different concentrations. All images are taken at ×20 magnification with Carl Zeiss phase contrast microscope. Scale bars, 100 μm

Figure 5: (a) Representative histogram showing <i>in vitro</i> dose-dependent cytotoxicity of (A) aqueous extract of leaves, bark, and flowers on MCF-7 cells exposed for 24 h, (B) MCF-7 cells exposed to methanol extracts of plant parts exposed for 24 h, (C) MCF-7 cells exposed to ethanol extracts for 24 h, (D) MCF-7 cells exposed to aqueous extracts of plant parts exposed for 48 h, (E) MCF-7 cells exposed to methanol extracts of plant parts exposed for 48 h (F) MCF-7 cells exposed to ethanol extracts of plant parts exposed for 48 h. The results represent the means of three independent experiments, and error bars represent the standard error of the mean. (b) Cell morphology of MCF-7 cells after 48 h treatment of aqueous, methanol, and ethanol extracts of leaves, stem bark, and flowers of <i>Lasiosiphon eriocephalus</i> at different concentrations. All images are taken at ×20 magnification with Carl Zeiss phase contrast microscope. Scale bars, 100 μm. (c) Representative histogram showing <i>in vitro</i> dose dependent cytotoxicity of (A) aqueous extract of leaves, bark and flowers on HeLa cells exposed for 24 h, (B) HeLa cells exposed to methanol extracts of plant parts exposed for 24 h, (C) HeLa cells exposed to ethanol extracts for 24 h, (D) HeLa cells exposed to aqueous extracts of plant parts exposed for 48 h, (E) HeLa cells exposed to methanol extracts of plant parts exposed for 48 h (F) HeLa cells exposed to ethanol extracts of plant parts exposed for 48 h. The results represent the means of three independent experiments, and error bars represent the standard error of the mean. (d) Cell morphology of HeLacells after 48 h treatment of aqueous, methanol, and ethanol extracts of leaves, stem bark, and flowers of <i>Lasiosiphon eriocephalus</i> at different concentrations. All images are taken at ×20 magnification with Carl Zeiss phase contrast microscope. Scale bars, 100 μm