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  1. Article ; Online: A novel and unusual utility of the cardiosintol drug as a fluoro-prober in the amendment of a highly fluorescent module for determining the non-fluorescent N-acetylcysteine drug.

    Hamad, Ahmed A / Derayea, Sayed M

    Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy

    2023  Volume 293, Page(s) 122460

    Abstract: It is common to use reagents to determine the drugs by exploiting the properties of these reagents in the development of fluorescence of the target drug or sometimes increasing its intensity; this is the usual and predominant in the methods used in ... ...

    Abstract It is common to use reagents to determine the drugs by exploiting the properties of these reagents in the development of fluorescence of the target drug or sometimes increasing its intensity; this is the usual and predominant in the methods used in various techniques. But using a drug as a reagent to analyze another drug is unique, unusual, and uncommon; that's the idea of this paper. This is possible by creating a chemical modulation in the drug's structure using another drug. Targeted analyte molecules (N-acetylcysteine, as an example) that lack fluorogenic or chromophoric moieties cannot be monitored or evaluated without undergoing structural modification. Thus, the chemical mending of the analyte's molecular structure can achieve the transformational process. This protocoled analytical method generates an amended fluorescence sensation that can be chased fluorimetrically at 441 nm (emission) following excitation at 339 nm. When o-dialdehyde, diformylbenzene, a non-fluorescent moiety, is added to a solution of non-fluorescent analyte in the presence of cardiosintol drug, at a specific pH, the target drug-thiol moiety can be amended into a highly fluorescent compound. This study presented a sensitive and feasible fluorometric test for acetylcysteine. The response is linear throughout the range of 0.05-0.80 µg mL
    MeSH term(s) Acetylcysteine ; Indicators and Reagents ; Coloring Agents ; Spectrometry, Fluorescence ; Molecular Structure ; Fluorescent Dyes/chemistry
    Chemical Substances Acetylcysteine (WYQ7N0BPYC) ; Indicators and Reagents ; Coloring Agents ; Fluorescent Dyes
    Language English
    Publishing date 2023-02-08
    Publishing country England
    Document type Journal Article
    ZDB-ID 210413-1
    ISSN 1873-3557 ; 0370-8322 ; 0584-8539 ; 1386-1425
    ISSN (online) 1873-3557
    ISSN 0370-8322 ; 0584-8539 ; 1386-1425
    DOI 10.1016/j.saa.2023.122460
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: The first spectrofluorimetric protocol for sensitive quantitative analysis of bromocriptine in its pure and pharmaceutical forms: evaluation of the greenness of the method.

    Abdulrazik, Shrouk G / Attia, Tamer Z / Derayea, Sayed M

    RSC advances

    2023  Volume 13, Issue 50, Page(s) 35733–35740

    Abstract: Bromocriptine mesylate, a dopamine ... ...

    Abstract Bromocriptine mesylate, a dopamine D
    Language English
    Publishing date 2023-12-08
    Publishing country England
    Document type Journal Article
    ISSN 2046-2069
    ISSN (online) 2046-2069
    DOI 10.1039/d3ra06626f
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: Quantitative spectrofluorimetric method for determination of octreotide acetate synthetic peptide derivative in pure and its Sandostatin ampules forms.

    Derayea, Sayed M / Abdulrazik, Shrouk G / Attia, Tamer Z

    Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy

    2023  Volume 305, Page(s) 123546

    Abstract: A unique spectrofluorimetric protocol has been conceived for octreotide (a synthetic peptide drug) quantitation in both its authentic form and its application to dosage form. The protocol has been established simply upon condensation of octreotide by ... ...

    Abstract A unique spectrofluorimetric protocol has been conceived for octreotide (a synthetic peptide drug) quantitation in both its authentic form and its application to dosage form. The protocol has been established simply upon condensation of octreotide by ninhydrin / phenyl acetaldehyde reagent in buffered media (pH 6.2). An intense fluorescence product has been formed and quantified at 463 nm (390 nm for excitation). After optimization for various experimental conditions, a wide linear interval (0.2-4.0 µg/ml) has been used to construct the calibration curve with a determination coefficient (r
    MeSH term(s) Octreotide ; Spectrometry, Fluorescence/methods ; Indicators and Reagents ; Ninhydrin
    Chemical Substances Octreotide (RWM8CCW8GP) ; Indicators and Reagents ; Ninhydrin (HCL6S9K23A)
    Language English
    Publishing date 2023-10-16
    Publishing country England
    Document type Journal Article
    ZDB-ID 210413-1
    ISSN 1873-3557 ; 0370-8322 ; 0584-8539 ; 1386-1425
    ISSN (online) 1873-3557
    ISSN 0370-8322 ; 0584-8539 ; 1386-1425
    DOI 10.1016/j.saa.2023.123546
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: Development of a green synchronous spectrofluorimetric technique for simultaneous determination of Montelukast sodium and Bilastine in pharmaceutical formulations.

    Derayea, Sayed M / Badr El-Din, Khalid M / Ahmed, Ahmed S / Khorshed, Ahmed A / Oraby, Mohamed

    BMC chemistry

    2024  Volume 18, Issue 1, Page(s) 18

    Abstract: For the treatment of rhinitis and asthma, a combination of Montelukast sodium and Bilastine has just been approved. Based on the first derivative of synchronous fluorescence, the current work developed a green, highly accurate, sensitive, and selective ... ...

    Abstract For the treatment of rhinitis and asthma, a combination of Montelukast sodium and Bilastine has just been approved. Based on the first derivative of synchronous fluorescence, the current work developed a green, highly accurate, sensitive, and selective spectroscopic approach for estimating Montelukast sodium and Bilastine in pharmaceutical dosage form without previous separation. The selected technique focuses on measuring the synchronized fluorescence of the studied medications at a fixed wavelength range (Δλ) = 110 nm, and using the amplitude of the first derivative's peak at 381 and 324 nm, for quantitative estimation of Montelukast sodium and Bilastine, respectively. The impacts of different factors on the referred drugs' synchronized fluorescence intensity were investigated and adjusted. The calibration plots for were found to be linear over concentration ranges of 50-2000 ng mL
    Language English
    Publishing date 2024-01-25
    Publishing country Switzerland
    Document type Journal Article
    ISSN 2661-801X
    ISSN (online) 2661-801X
    DOI 10.1186/s13065-024-01116-3
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: Novel spectrofluorometric approach for assessing vilazodone by blocking photoinduced electron transfer: analytical performance, and greenness-blueness evaluation.

    Derayea, Sayed M / Elhamdy, Hadeer A / Badr El-Din, Khalid M / Oraby, Mohamed

    RSC advances

    2024  Volume 14, Issue 6, Page(s) 4065–4073

    Abstract: In this paper, vilazodone (VLD), a serotonin modulator prescribed for major depressive disorder, was investigated using a rapid, highly sensitive, and eco-friendly spectrofluorometric approach. The native fluorescence of VLD, originating from its indole ... ...

    Abstract In this paper, vilazodone (VLD), a serotonin modulator prescribed for major depressive disorder, was investigated using a rapid, highly sensitive, and eco-friendly spectrofluorometric approach. The native fluorescence of VLD, originating from its indole moiety, exhibited an emission peak at 486 nm upon excitation at 241 nm. However, the presence of a piperazinyl nitrogen atom in the VLD structure, acting as an electron donor, significantly diminished the fluorescence intensity through photoinduced electron transfer (PET) to the indole ring. However, by protonating this nitrogen atom using 0.02 M Teorell-Stenhagen buffer (pH 3.5), inhibition of the PET process effectively blocked electron transfer, restoring the fluorescent properties of the drug. Further, an enhancement in the fluorescence was achieved by employing methanol as the solvent, resulting in a 1.5-fold increase. The combined use of PET blockage and methanol enabled the detection of VLD at levels as low as 0.78 ng mL
    Language English
    Publishing date 2024-01-29
    Publishing country England
    Document type Journal Article
    ISSN 2046-2069
    ISSN (online) 2046-2069
    DOI 10.1039/d3ra08034j
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article ; Online: An eco-friendly one-pot spectrofluorimetric approach for the facile determination of overactive bladder drug, tolterodine: Application to dosage forms and biological fluids.

    Derayea, Sayed M / Badr El-Din, Khalid M / Ahmed, Ahmed S / Abdelshakour, Mohamed A / Oraby, Mohamed

    Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy

    2024  Volume 311, Page(s) 123986

    Abstract: Tolterodine tartrate (TTD) was the first antimuscarinic medication developed exclusively for the treatment of overactive bladder syndrome and was approved by the FDA in 1998. As a result of the drug's extensive utilization within the local community ... ...

    Abstract Tolterodine tartrate (TTD) was the first antimuscarinic medication developed exclusively for the treatment of overactive bladder syndrome and was approved by the FDA in 1998. As a result of the drug's extensive utilization within the local community following its authorization, there is a pressing need to develop and validate a spectrofluorometric method that is economically efficient, easily reproducible, environmentally sustainable, and possesses high sensitivity. The developed approach relies on enhancing the fluorescence intensity of TTD to reach a level 720 % higher than its initial value, achieved through the application of an aqueous sodium dodecyl sulfate (SDS) solution. A strong correlation was observed with a correlation coefficient of 0.9998 between the concentration of TTD and the fluorescence intensity within the range of 25.0-500.0 ng mL
    MeSH term(s) Humans ; Tolterodine Tartrate ; Urinary Bladder, Overactive/drug therapy ; Spectrometry, Fluorescence/methods ; Muscarinic Antagonists/therapeutic use ; Sodium Dodecyl Sulfate
    Chemical Substances Tolterodine Tartrate (5T619TQR3R) ; Muscarinic Antagonists ; Sodium Dodecyl Sulfate (368GB5141J)
    Language English
    Publishing date 2024-02-04
    Publishing country England
    Document type Journal Article
    ZDB-ID 210413-1
    ISSN 1873-3557 ; 0370-8322 ; 0584-8539 ; 1386-1425
    ISSN (online) 1873-3557
    ISSN 0370-8322 ; 0584-8539 ; 1386-1425
    DOI 10.1016/j.saa.2024.123986
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article ; Online: Determination of antihistaminic drugs alcaftadine and olopatadine hydrochloride via ion-pairing with eosin Y as a spectrofluorimetric and spectrophotometric probe: application to dosage forms.

    Derayea, Sayed M / Badr El-Din, Khalid M / Ahmed, Ahmed S / Khorshed, Ahmed A / Oraby, Mohamed

    BMC chemistry

    2024  Volume 18, Issue 1, Page(s) 40

    Abstract: Four sensitive and fast analytical approaches relied on ion pairing with eosin Y were built up and evaluated using spectroscopy for determination of Alcaftadine and Olopatadine hydrochloride with high sensitivity and selectivity. Two spectrofluorimetric ... ...

    Abstract Four sensitive and fast analytical approaches relied on ion pairing with eosin Y were built up and evaluated using spectroscopy for determination of Alcaftadine and Olopatadine hydrochloride with high sensitivity and selectivity. Two spectrofluorimetric techniques were employed to observe the quenching effect of Alcaftadine or Olopatadine hydrochloride on the intrinsic fluorescence of eosin Y in a 0.1 M acetate buffer solution at pH 3.8 and 3.3 for Alcaftadine and Olopatadine hydrochloride, respectively. Those methods are considered the first spectrofluorimetric methods for Alcaftadine and Olopatadine hydrochloride assay. The fluorescence quenching effect was linear with concentration ranging from 150 to 2000 and 200 to 2000 ng mL
    Language English
    Publishing date 2024-02-22
    Publishing country Switzerland
    Document type Journal Article
    ISSN 2661-801X
    ISSN (online) 2661-801X
    DOI 10.1186/s13065-024-01137-y
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article ; Online: Integrated resonance Rayleigh scattering approach utilizing Box-Behnken experimental design for the facile quantification of prucalopride in pharmaceutical tablets and human urine with sustainability assessment.

    Badr El-Din, Khalid M / Derayea, Sayed M / Mohammed, Fatma F / Hamad, Ahmed Abdulhafez

    RSC advances

    2024  Volume 14, Issue 11, Page(s) 7797–7805

    Abstract: Prucalopride (PCP) is one of the recent drugs used for the regulation of gastrointestinal tract motility and the treatment of constipation. A new, highly sensitive and fast resonance Rayleigh scattering (RRS) approach was suggested for PCP determination. ...

    Abstract Prucalopride (PCP) is one of the recent drugs used for the regulation of gastrointestinal tract motility and the treatment of constipation. A new, highly sensitive and fast resonance Rayleigh scattering (RRS) approach was suggested for PCP determination. The approach was based on its reaction of PCP with eosin Y in buffered medium (pH 3.5) to form an ion pair association complex which had a significant enhancement in RRS compared to that of eosin Y or PCP alone. The enhancement of RRS intensity had straight correlation to PCP concentration ranging from 150 to 2000 ng mL
    Language English
    Publishing date 2024-03-05
    Publishing country England
    Document type Journal Article
    ISSN 2046-2069
    ISSN (online) 2046-2069
    DOI 10.1039/d3ra07980e
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  9. Article ; Online: A facile on-off fluorescence approach for fluvoxamine determination in pharmaceutical tablets; application to content uniformity testing.

    Derayea, Sayed M / Oraby, Mohamed / Zaafan, Al Amir S / Hamad, Ahmed Abdulhafez / Nagy, Dalia M

    RSC advances

    2024  Volume 14, Issue 12, Page(s) 8283–8292

    Abstract: A green-complied spectrofluorimetric approach for quantification of the antidepressant, fluvoxamine, has been established. The method that has been suggested relies on the development of an association complex between fluvoxamine and erythrosine B in an ... ...

    Abstract A green-complied spectrofluorimetric approach for quantification of the antidepressant, fluvoxamine, has been established. The method that has been suggested relies on the development of an association complex between fluvoxamine and erythrosine B in an acetate buffer solution. After being excited at 530 nm, the quenching in erythrosine B's native fluorescence caused by complex formation with fluvoxamine was detected at a wavelength of 552 nm. The values of fluorescence quenching at the most optimal reaction conditions were rectilinear at the concentration range of 0.2-2.0 μg mL
    Language English
    Publishing date 2024-03-11
    Publishing country England
    Document type Journal Article
    ISSN 2046-2069
    ISSN (online) 2046-2069
    DOI 10.1039/d3ra08257a
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  10. Article ; Online: Sensitive spectrofluorimetric determination of the prokinetic drug prucalopride succinate based on supramolecular aggregation approach with evaluation of method greenness: application to content uniformity test.

    Derayea, Sayed M / Mohammed, Fatma F / Badr El-Din, Khalid M

    Luminescence : the journal of biological and chemical luminescence

    2023  Volume 38, Issue 12, Page(s) 2065–2072

    Abstract: The prokinetic drug, prucalopride (PCP) succinate, was determined using a new spectrofluorimetric approach with a highly sensitive, rapid, and simple procedure. The method exploited the enhancement of the inherent native fluorescence of PCP by micellar ... ...

    Abstract The prokinetic drug, prucalopride (PCP) succinate, was determined using a new spectrofluorimetric approach with a highly sensitive, rapid, and simple procedure. The method exploited the enhancement of the inherent native fluorescence of PCP by micellar aggregation with sodium lauryl sulfate (SLS) as an anionic surfactant. Different factors that could affect the fluorescence intensity were carefully studied in order to achieve the maximal fluorescence signal. Measurement of the enhanced fluorescence was done at 354 nm after the excitation at 276 nm. The fluorescence intensity-concentration plot was rectilinear in the concentration range of 50-600 ng/ml with detection and quantitation limits of 13.9 and 42.1 ng/ml, respectively. The method underwent validation according to the International Council for Harmonisation criteria in order to assess its analytical performance, and promising results were achieved that proved the validity and reliability of the method. Furthermore, the method was employed effectively for the analysis of the cited drug in commercial pharmaceutical tablets.
    MeSH term(s) Limit of Detection ; Spectrometry, Fluorescence/methods ; Reproducibility of Results ; Succinates ; Tablets/analysis
    Chemical Substances prucalopride (0A09IUW5TP) ; Succinates ; Tablets
    Language English
    Publishing date 2023-10-10
    Publishing country England
    Document type Journal Article
    ZDB-ID 1470995-8
    ISSN 1522-7243 ; 1522-7235 ; 1099-1271
    ISSN (online) 1522-7243
    ISSN 1522-7235 ; 1099-1271
    DOI 10.1002/bio.4597
    Database MEDical Literature Analysis and Retrieval System OnLINE

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