Optimization of a Microwell cytotoxicity assay using Artemia salina (brine shrimps) / Myra Sharon Malicsi

By: Material type: TextTextLanguage: English Publication details: 2000Description: 25 leavesSubject(s): Dissertation note: Thesis (BS Biology) -- University of the Philippines Mindanao, 2000 Summary: The microwell cytotoxicity assay using Artemia salina (brine shrimps) was done as follows: (1) Artemia salina cysts, 0.25 grams, was hatched in 100 ml artificially prepared seawater supplemented with 0.006 grams of yeast extract, (2) continuous moderate aeration was provided in the culture media, (3) serial dilutions of chloramphenicol, cyclohexanone and vincristine were made in the well of the 96-microwell plate, (4) a suspension containing 10-15 nauplii was added tp each well. (5) after 24 hours of hydration, the number of dead nauplii per well was counted, and (6) media lethal concentration was determined using the Probit analysis. It was found that efficiency and rate of hatching increased with salt concentration in the culture media. The 24 hr. LC50 of chloramphenicol, cyclohexanone and vincristine were 39450.12 mg/ml, 5007.907 mg/ml and 1023.712 mg/ml, respectively
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Item type Current library Collection Call number Status Date due Barcode
Thesis University Library Non-Circulation LG993.5 2000 B4 M35 (Browse shelf(Opens below)) Available 3UPML00020854
Thesis University Library Reference/Room-Use Only LG993.5 2000 B4 M35 (Browse shelf(Opens below)) Available 3UPML00010998

Thesis (BS Biology) -- University of the Philippines Mindanao, 2000

The microwell cytotoxicity assay using Artemia salina (brine shrimps) was done as follows: (1) Artemia salina cysts, 0.25 grams, was hatched in 100 ml artificially prepared seawater supplemented with 0.006 grams of yeast extract, (2) continuous moderate aeration was provided in the culture media, (3) serial dilutions of chloramphenicol, cyclohexanone and vincristine were made in the well of the 96-microwell plate, (4) a suspension containing 10-15 nauplii was added tp each well. (5) after 24 hours of hydration, the number of dead nauplii per well was counted, and (6) media lethal concentration was determined using the Probit analysis. It was found that efficiency and rate of hatching increased with salt concentration in the culture media. The 24 hr. LC50 of chloramphenicol, cyclohexanone and vincristine were 39450.12 mg/ml, 5007.907 mg/ml and 1023.712 mg/ml, respectively

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