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. Author manuscript; available in PMC: 2006 Aug 30.
Published in final edited form as: J Agric Food Chem. 2006 Apr 19;54(8):2881–2890. doi: 10.1021/jf052344k

Table 4.

Cytotoxicity of Extract Stock Solutions from Dried Frontier Herb Hp in Three Cancer Cell Linesa

mean ± SE
NIH3T3 mouse fibroblasts
SW480 human colon cancer cells
HaCaT human skin keratinocytes
extraction method and solvents (treatment concn of extracts in media) light dark light dark light dark
Soxhlet
100% EtOH (1161 μg/mL) 7.7** (±4.2) 10.3** (±4.9) 8.3** (±3.5) 11.7** (±2.8) 35.4** (±7.5) 40.3** (±8.9)
chloroform (284 μg/mL) 5.5** (±3.7) 9.0** (±5.1) 2.5** (±1.7) 8.2** (±4.1) 1.6** (±1.1) 0.4** (±0.2)
hexane (166 μg/mL) 3.1** (±2.0) 4.1** (±2.6) 1.5** (±1.3) 2.9** (±2.5) 0.3** (±0.3) 0.3** (±0.3)
100% ethanol (–chloroform) (589 μg/mL) 38.1* (±3.4) 49.0* (±3.3) 55.1** ## (±2.7) 77.2 (±1.2) 35.6** ## (±6.8) 77.4* (±9.9)
100% ethanol (–hexane) (568 μg/mL) 12.0** ## (± 4.6) 32.5** (± 3.1) 8.7** ## (± 2.7) 32.4** (± 4.9) 40.8** (± 11.8) 50.4** (± 9.6)
room temperature shaking
70% EtOH (740 μg/mL) 11.1** (±9.1) 12.5** (±7.4) 2.5** (±0.9) 14.2** (±5.5) 42.8** (±8.9) 34.3** (±10.6)
chloroform (174 μg/mL) 34.8** (±6.5) 33.1** (±6.7) 26.8** (±11.8) 47.6* (±5.2) 8.5** (±5.1) 12.1** (±2.9)
hexane (58 μg/mL) 82.6 (±1.9) 81.4 (±2.9) 83.3 (±9.0) 88.5 (±2.4) 89.5 (±4.9) 94.1 (±3.6)
70% ethanol (–chloroform) (692 μg/mL) 33.6** (±7.4) 27.6** (±6.7) 57.7** (±7.5) 44.6** (±6.7) 41.6** (±3.6) 66.2* (±13.7)
70% ethanol (–hexane) (556 μg/mL) 29.7** (±8.5) 35.1** (±6.1) 25.0** (±4.9) 39.2** (±8.2) 32.9** (±7.8) 45.4** (±9.4)
water (213 μg/mL) 84.4* (±3.0) 85.5* (±1.7) 95.6 (±5.0) 85.1 (±5.7) 73.6 (±16.2) 87.7 (±8.1)
20 μM hypericin 10.1** ## (±6.2) 60.9** (±5.7) 20.8** ## (±2.4) 80.5 (±1.3) 0.87** # (±0.4) 53.2** (±10.9)
a

Cytotoxicity (% survival as compared to vehicle control-treated cells) of Hp extracts screened via the Celltiter96 Aqueous One Solution Cytotoxicity assay (n = 3–5). All extract stock solutions were prepared from 6 g (water extract from 5 g) of dried plant material by either Soxhlet or room temperature extraction and included as 1% of the cell culture media. One set of chloroform and hexane extracts was sequentially extracted in ethanol:ethanol(–chloroform) or ethanol(–hexane). The treatment concentration listed for each extract or fraction (μg/mL) is the amount of extract residue obtained after extraction, diluted in DMSO, and used in the assay. A 20 μM concentration of hypericin was the positive control.

**

= p < 0.0001 and

*

= p < 0.01 significantly different cell growth survival as compared to DMSO solvent control.

##

= p < 0.0001 and

#

= p < 0.01 significantly different cell growth survival after exposure to 30 min of ambient light as compared to the dark incubation.