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14 results for “Quinabut”
Figure 6 from: Golembiovska О, Voskoboinik O, Berest G, Kovalenko S, Logoyda L (2021) Quality by design approach for simultaneous determination of original active pharmaceutical ingredient quinabut and its impurities by using HPLC. Message 1. Pharmacia 68(1): 79-87. https://doi.org/10.3897/pharmacia.68.e50704
Figure 6 Linear dependence of the theoretical concentration of quinabut on the found concentration in normalized coordinates.
Supplementary material 1 from: Golembiovska О, Voskoboinik O, Berest G, Kovalenko S, Logoyda L (2021) Quality by design approach for simultaneous determination of original active pharmaceutical ingredient quinabut and its impurities by using HPLC. Message 1. Pharmacia 68(1): 79-87. https://doi.org/10.3897/pharmacia.68.e50704
Shimadzu LCsolution Analysis Report
Figure 6 from: Golembiovska О, Voskoboinik O, Berest G, Kovalenko S, Logoyda L (2021) Method development and validation for the determination of residual solvents in quinabut API by using gas chromatography. Message 2. Pharmacia 68(1): 53-59. https://doi.org/10.3897/pharmacia.68.e52119
Figure 6 Linearity of IPA solutions.
Figure 5 from: Golembiovska О, Voskoboinik O, Berest G, Kovalenko S, Logoyda L (2021) Method development and validation for the determination of residual solvents in quinabut API by using gas chromatography. Message 2. Pharmacia 68(1): 53-59. https://doi.org/10.3897/pharmacia.68.e52119
Figure 5 Linearity of acetone solutions.
Figure 4 from: Golembiovska О, Voskoboinik O, Berest G, Kovalenko S, Logoyda L (2021) Method development and validation for the determination of residual solvents in quinabut API by using gas chromatography. Message 2. Pharmacia 68(1): 53-59. https://doi.org/10.3897/pharmacia.68.e52119
Figure 4 Chromatogram of specificity (spiked solution of quinabut API, acetone and 2-propanol).
Figure 3 from: Golembiovska О, Voskoboinik O, Berest G, Kovalenko S, Logoyda L (2021) Method development and validation for the determination of residual solvents in quinabut API by using gas chromatography. Message 2. Pharmacia 68(1): 53-59. https://doi.org/10.3897/pharmacia.68.e52119
Figure 3 Typical chromatogram of acetone and IPA standard solution.
Figure 2 from: Golembiovska О, Voskoboinik O, Berest G, Kovalenko S, Logoyda L (2021) Method development and validation for the determination of residual solvents in quinabut API by using gas chromatography. Message 2. Pharmacia 68(1): 53-59. https://doi.org/10.3897/pharmacia.68.e52119
Figure 2 Typical chromatogram of blank (water).
Figure 1 from: Golembiovska О, Voskoboinik O, Berest G, Kovalenko S, Logoyda L (2021) Method development and validation for the determination of residual solvents in quinabut API by using gas chromatography. Message 2. Pharmacia 68(1): 53-59. https://doi.org/10.3897/pharmacia.68.e52119
Figure 1 Chemical structure of quinabut.
Figure 7 from: Golembiovska О, Voskoboinik O, Berest G, Kovalenko S, Logoyda L (2021) Method development and validation for the determination of residual solvents in quinabut API by using gas chromatography. Message 2. Pharmacia 68(1): 53-59. https://doi.org/10.3897/pharmacia.68.e52119
Figure 7 Chromatogram of quinabut API sample.
Figure 2 from: Golembiovska О, Voskoboinik O, Berest G, Kovalenko S, Logoyda L (2021) Quality by design approach for simultaneous determination of original active pharmaceutical ingredient quinabut and its impurities by using HPLC. Message 1. Pharmacia 68(1): 79-87. https://doi.org/10.3897/pharmacia.68.e50704
Figure 2 UV spectrum of quinabut.
Figure 5 from: Golembiovska О, Voskoboinik O, Berest G, Kovalenko S, Logoyda L (2021) Quality by design approach for simultaneous determination of original active pharmaceutical ingredient quinabut and its impurities by using HPLC. Message 1. Pharmacia 68(1): 79-87. https://doi.org/10.3897/pharmacia.68.e50704
Figure 5 Chromatogram of the test solution (a) after exposure to UV light.
Figure 4 from: Golembiovska О, Voskoboinik O, Berest G, Kovalenko S, Logoyda L (2021) Quality by design approach for simultaneous determination of original active pharmaceutical ingredient quinabut and its impurities by using HPLC. Message 1. Pharmacia 68(1): 79-87. https://doi.org/10.3897/pharmacia.68.e50704
Figure 4 Chromatogram of blank solution.
Figure 3 from: Golembiovska О, Voskoboinik O, Berest G, Kovalenko S, Logoyda L (2021) Quality by design approach for simultaneous determination of original active pharmaceutical ingredient quinabut and its impurities by using HPLC. Message 1. Pharmacia 68(1): 79-87. https://doi.org/10.3897/pharmacia.68.e50704
Figure 3 Chromatogram of the test solution.
Figure 1 from: Golembiovska О, Voskoboinik O, Berest G, Kovalenko S, Logoyda L (2021) Quality by design approach for simultaneous determination of original active pharmaceutical ingredient quinabut and its impurities by using HPLC. Message 1. Pharmacia 68(1): 79-87. https://doi.org/10.3897/pharmacia.68.e50704
Figure 1 Chemical structures of quinabut (I) and impurity A (II).
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