Radioprotective potential of leea manillensis syn. Guineensis (abang-abang) leaf extract on gamma-irradiated human blood lymphocytesn in vitro / Charlotte F. Marasigan. 6

By: Charlotte F. Marasigan. 4 0 16, [, ] | [, ] |
Contributor(s): 5 6 [] |
Language: Unknown language code Summary language: Unknown language code Original language: Unknown language code Series: ; March 2017.46Edition: Description: 28 cm. 31 ppContent type: text Media type: unmediated Carrier type: volumeISBN: ISSN: 2Other title: 6 []Uniform titles: | | Related works: 1 40 6 []Subject(s): -- 2 -- 0 -- -- | -- 2 -- 0 -- 6 -- | 2 0 -- | -- -- 20 -- | | -- -- -- -- 20 -- | -- -- -- 20 -- --Genre/Form: -- 2 -- Additional physical formats: DDC classification: | LOC classification: | | 2Other classification:
Contents:
Action note: In: Summary: ABSTRACT: The objective of the study was to evaluate the Radioprotective Potential of Leea manillensis syn. guineensis (Abang-abang) extract on gamma irradiated human lymphocytes in vitro using the micronucleus assay. The 100% pure concentration of Leea manillensis syn. guineensis (Abang-abang) extract was diluted into varying concentration of 0.1 mg/ml, 0.2 mg/ml, 0.3 mg/ml, and 0.4 mg/ml which were added to the irradiated blood samples. Based on the experiment, the extract of Leea manillensis syn, guineensis (Abang-abang) reduced the number of the micronuclei in the 1000 binucleated cells. Hoewever only 0.4 mg/ml of Leea manillensis syn. guineenis (Abang-abang) exhibited the greatest radioprotective activity in terms of the reduced micronucleus formation. One-way analysis of variance (ANOVA) was utilized to determine and evaluate if there is a significant difference between the experimental group. It demonstrated that the Leea manillensis syn. guineesis (Abang-abang) extract reduced the number of micronuclei and the highest plant concentration which was 0.4 mg/ml yielded the least number of micronuclei which was 0.4 mg/ml yielded the least number of micronuclei which scored a mean of 33. Furthermore, it was observed and evident that the 0.4 mg/ml plant concentration had no significant difference (p<0.05) from the positive control, oregano extract. Other editions:
Tags from this library: No tags from this library for this title. Log in to add tags.
    Average rating: 0.0 (0 votes)
Item type Current location Home library Collection Call number Status Date due Barcode Item holds
Book PLM
PLM
Filipiniana Section
Filipiniana-Thesis T QH450.M37.2017 (Browse shelf) Available FT6239
Total holds: 0

Thesis:(B.S. Biology)-Pamantasan ng Lungsod ng Maynila, 2017. 56

5

ABSTRACT: The objective of the study was to evaluate the Radioprotective Potential of Leea manillensis syn. guineensis (Abang-abang) extract on gamma irradiated human lymphocytes in vitro using the micronucleus assay. The 100% pure concentration of Leea manillensis syn. guineensis (Abang-abang) extract was diluted into varying concentration of 0.1 mg/ml, 0.2 mg/ml, 0.3 mg/ml, and 0.4 mg/ml which were added to the irradiated blood samples. Based on the experiment, the extract of Leea manillensis syn, guineensis (Abang-abang) reduced the number of the micronuclei in the 1000 binucleated cells. Hoewever only 0.4 mg/ml of Leea manillensis syn. guineenis (Abang-abang) exhibited the greatest radioprotective activity in terms of the reduced micronucleus formation. One-way analysis of variance (ANOVA) was utilized to determine and evaluate if there is a significant difference between the experimental group. It demonstrated that the Leea manillensis syn. guineesis (Abang-abang) extract reduced the number of micronuclei and the highest plant concentration which was 0.4 mg/ml yielded the least number of micronuclei which was 0.4 mg/ml yielded the least number of micronuclei which scored a mean of 33. Furthermore, it was observed and evident that the 0.4 mg/ml plant concentration had no significant difference (p<0.05) from the positive control, oregano extract.

5

There are no comments for this item.

to post a comment.

© Copyright 2024 Phoenix Library Management System - Pinnacle Technologies, Inc. All Rights Reserved.