PEG-calf thymus DNA interactions: Conformational, morphological and spectroscopic thermal studies
被引:12
作者:
Adali, Terin
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机构:
Near East Univ, Dept Biomed Engn, Lefkosa North Cyprus, TurkeyNear East Univ, Dept Biomed Engn, Lefkosa North Cyprus, Turkey
Adali, Terin
[1
]
Bentaleb, Ali
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Near East Univ, Dept Biomed Engn, Lefkosa North Cyprus, TurkeyNear East Univ, Dept Biomed Engn, Lefkosa North Cyprus, Turkey
Bentaleb, Ali
[1
]
Elmarzugi, Nagib
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机构:
Univ Teknol Malaysia, Inst Bioprod Dev, Utm 81310, Johor, Malaysia
Tripoli Univ, Fac Pharm, Dept Ind Pharm, Tripoli, LibyaNear East Univ, Dept Biomed Engn, Lefkosa North Cyprus, Turkey
Elmarzugi, Nagib
[2
,3
]
Hamza, Amal M.
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Natl Med Res Ctr, NASR, Alzawia, LibyaNear East Univ, Dept Biomed Engn, Lefkosa North Cyprus, Turkey
Hamza, Amal M.
[4
]
机构:
[1] Near East Univ, Dept Biomed Engn, Lefkosa North Cyprus, Turkey
[2] Univ Teknol Malaysia, Inst Bioprod Dev, Utm 81310, Johor, Malaysia
[3] Tripoli Univ, Fac Pharm, Dept Ind Pharm, Tripoli, Libya
The main aim of this study is to provide understanding for the interaction modes and the binding affinity based on the study of PEG 400 that binds to ctDNA. The effects of the PEG-400-to-ctDNA ratio, pH, incubation time and thermal stability of ctDNA on PEG-ctDNA biocomplex formation were studied. UV-vis-NIR absorption analysis indicated that PEG forms a complex with ctDNA via a mechanism other than intercalation. The results of thermal denaturation studies showed that the PEG-ctDNA biocomplex helix was stabilised, with a resulting increase in the PEG-ctDNA melting temperature. FTIR analysis indicated that the PEG binds to ctDNA through weak to moderately strong hydrophilic and hydrophobic interactions with the base pairs of ctDNA. TEM micrographs showed that the addition of PEG to ctDNA caused ctDNA to condense with PEG molecules into an irregular aggregate structure. These results demonstrate that the PEG-ctDNA biocomplex has potential applications in biomedical sciences. (C) 2013 Elsevier B.V. All rights reserved.
机构:
Kermanshah Univ Med Sci, Fac Pharm, Dept Med Chem, Kermanshah 671451673, IranKermanshah Univ Med Sci, Fac Pharm, Dept Med Chem, Kermanshah 671451673, Iran
Ahmadi, F.
;
Alizadeh, A. A.
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Kermanshah Univ Med Sci, Fac Pharm, Dept Med Chem, Kermanshah 671451673, IranKermanshah Univ Med Sci, Fac Pharm, Dept Med Chem, Kermanshah 671451673, Iran
Alizadeh, A. A.
;
Shahabadi, N.
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机构:
Razi Univ, Fac Sci, Dept Chem, Kermanshah, IranKermanshah Univ Med Sci, Fac Pharm, Dept Med Chem, Kermanshah 671451673, Iran
Shahabadi, N.
;
Rahimi-Nasrabadi, M.
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机构:
Imam Hossein Univ, Dept Chem, Tehran, IranKermanshah Univ Med Sci, Fac Pharm, Dept Med Chem, Kermanshah 671451673, Iran
机构:Univ Utah, Ctr Controlled Chem Delivery, Dept Pharmaceut & Pharmaceut Chem, Salt Lake City, UT 84112 USA
Lee, M
;
Kim, SW
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机构:
Univ Utah, Ctr Controlled Chem Delivery, Dept Pharmaceut & Pharmaceut Chem, Salt Lake City, UT 84112 USAUniv Utah, Ctr Controlled Chem Delivery, Dept Pharmaceut & Pharmaceut Chem, Salt Lake City, UT 84112 USA
机构:
Kermanshah Univ Med Sci, Fac Pharm, Dept Med Chem, Kermanshah 671451673, IranKermanshah Univ Med Sci, Fac Pharm, Dept Med Chem, Kermanshah 671451673, Iran
Ahmadi, F.
;
Alizadeh, A. A.
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机构:
Kermanshah Univ Med Sci, Fac Pharm, Dept Med Chem, Kermanshah 671451673, IranKermanshah Univ Med Sci, Fac Pharm, Dept Med Chem, Kermanshah 671451673, Iran
Alizadeh, A. A.
;
Shahabadi, N.
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机构:
Razi Univ, Fac Sci, Dept Chem, Kermanshah, IranKermanshah Univ Med Sci, Fac Pharm, Dept Med Chem, Kermanshah 671451673, Iran
Shahabadi, N.
;
Rahimi-Nasrabadi, M.
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h-index: 0
机构:
Imam Hossein Univ, Dept Chem, Tehran, IranKermanshah Univ Med Sci, Fac Pharm, Dept Med Chem, Kermanshah 671451673, Iran
机构:Univ Utah, Ctr Controlled Chem Delivery, Dept Pharmaceut & Pharmaceut Chem, Salt Lake City, UT 84112 USA
Lee, M
;
Kim, SW
论文数: 0引用数: 0
h-index: 0
机构:
Univ Utah, Ctr Controlled Chem Delivery, Dept Pharmaceut & Pharmaceut Chem, Salt Lake City, UT 84112 USAUniv Utah, Ctr Controlled Chem Delivery, Dept Pharmaceut & Pharmaceut Chem, Salt Lake City, UT 84112 USA