Nevirapine Pharmaceutical Cocrystal: Design, Development and Formulation

2019 ◽  
Vol 9 (3) ◽  
pp. 240-247
Author(s):  
Prabhakar Panzade ◽  
Priyanka Somani ◽  
Pavan Rathi
Keyword(s):  
Dosage Form ◽  
In Vitro Dissolution ◽  
Soluble Form ◽  
Ir Absorption ◽  
Stoichiometric Ratio ◽  
Design Development ◽  
Formulation Development ◽  
Scanning Calorimetry ◽  
Absorption Bands ◽  
Pharmaceutical Cocrystal

Background and Objective: The top approach to deliver poorly soluble drugs is the use of a highly soluble form. The present study was conducted to enhance the solubility and dissolution of a poorly aqueous soluble drug nevirapine via a pharmaceutical cocrystal. Another objective of the study was to check the potential of the nevirapine cocrystal in the dosage form. Methods: A neat and liquid assisted grinding method was employed to prepare nevirapine cocrystals in a 1:1 and 1:2 stoichiometric ratio of drug:coformer by screening various coformers. The prepared cocrystals were preliminary investigated for melting point and saturation solubility. The selected cocrystal was further confirmed by Infrared Spectroscopy (IR), Differential Scanning Calorimetry (DSC), and Xray Powder Diffraction (XRPD). Further, the cocrystal was subjected to in vitro dissolution study and formulation development. Results: The cocrystal of Nevirapine (NVP) with Para-Amino Benzoic Acid (PABA) coformer prepared by neat grinding in 1:2 ratio exhibited greater solubility. The shifts in IR absorption bands, alterations in DSC thermogram, and distinct XRPD pattern showed the formation of the NVP-PABA cocrystal. Dissolution of NVP-PABA cocrystal enhanced by 38% in 0.1N HCl. Immediate release tablets of NVP-PABA cocrystal exhibited better drug release and less disintegration time. Conclusion: A remarkable increase in the solubility and dissolution of NVP was obtained through the cocrystal with PABA. The cocrystal also showed great potential in the dosage form which may provide future direction for other drugs.

scholarly journals Изотопные эффекты в спектрах комплексов с водородными связями. Ангармонические расчеты изотопологов комплекса [F(HF)-=SUB=-2-=/SUB=-]-=SUP=---=/SUP=-

2020 ◽  
Vol 128 (8) ◽  
pp. 1077
Author(s):  
В.П. Булычев ◽  
М.В. Бутурлимова ◽  
К.Г. Тохадзе
Keyword(s):  
Basis Set ◽  
Ir Absorption ◽  
Absorption Bands ◽  
Spectral Parameters ◽  
Basis Set Superposition Error ◽  
Band Frequency ◽  
Normal Vibrations ◽  
K Meson ◽  
Anharmonic Interactions ◽  
Good Agreement

The frequencies and intensities of IR absorption bands of symmetric and asymmetric H-bonded complexes [FL1FL2F]- (L1, L2 = K-meson Ka, proton H, deuton D, and triton T) are calculated. The equilibrium configuration and potential energy and dipole moment surfaces of isotopologues [FL1FL2F]- were calculated by the MP2/6-311++G(3df,3pd) method with the basis set superposition error taken into account. The calculations of spectral parameters with allowance for anharmonic interactions of all vibrations were carried out using the second-order vibrational perturbation theory. Variation of Li and L2 masses in wide regions allowed significant changes in the forms of normal vibrations and values of anharmonic interaction constants upon isotopic substitution to be obtained. The trends in the changes of spectral parameters were determined upon transition from one symmetric isotopologue to another and upon transition from symmetric to asymmetric isotopologues. The D-F stretching band frequency predicted for [FHFDF]- is in good agreement with the experimental value. The assignment of this band was improved.

scholarly journals Local vibrational modes of vacancy-oxygen-related complexes at room temperature

2020 ◽  
Vol 56 (4) ◽  
pp. 480-487
Author(s):  
E. A. Tolkacheva ◽  
V. P. Markevich ◽  
L. I. Murin
Keyword(s):  
Absorption Band ◽  
Room Temperature ◽  
Clear Correlation ◽  
Ir Absorption ◽  
Oxygen Impurity ◽  
Interstitial Oxygen ◽  
Vibrational Modes ◽  
Oxygen Defect ◽  
Absorption Bands ◽  
Local Vibrational Modes

The isotopic content of natural silicon (28Si (92.23 %), 29Si (4.68 %) и 30Si (3.09 %)) affects noticeably the shape of IR absorption bands related to the oxygen impurity atoms. In the present work an attempt is undertaken to determine the positions of local vibrational modes (LVMs), related to quasimolecules 28Si16OS29Si and 28Si16OS30Si (OS – substitutional oxygen atom), for the absorption spectra measured at room temperature. An estimation of the isotopic shifts of corresponding modes is done by fitting the shape of the experimentally measured absorption band related to the vacancy–oxygen center in irradiated Si crystals. The LVM isotope shifts are found to be equal 2,2 ± 0.25 cm–1 for 28Si-16OS29Si and 4,3 ± 0,9 см–1 for 28Si-16OS30Si in relation to the basic band due to 28Si-16OS28Si, and the full width at half maximum of the A-center absorption band (28Si-16OS28Si) is 5,3 ± 0.25 cm–1. By means of infrared absorption spectroscopy a clear correlation between the disappearance of the divacancy (V2) in the temperature range 200–275 ºС and appearance of two absorption bands with their maxima at 825.8 and 839.2 cm–1 in irradiated oxygen-rich Si crystals is found. The band positioned at 825.8 cm–1 is assigned to a divacancy-oxygen defect V2O formed via an interaction of mobile V2 with interstitial oxygen (Oi ) atoms. The 839.2 cm–1 band is much more pronounced in neutron irradiated samples as compared to samples irradiated with electrons. We argue that it is related to a trivacancy–oxygen defect (V3O) formed via an interaction of mobile V3 with Oi atoms.

Magneto-Chemical Properties of Some New Ni and Co Rare-Earth Metal Tungstates

2007 ◽  
Vol 128 ◽  
pp. 207-212 ◽  
Author(s):  
Adam Worsztynowicz ◽  
Slawomir M. Kaczmarek ◽  
Elzbieta Tomaszewicz
Keyword(s):  
Rare Earth ◽  
Rare Earth Metal ◽  
Epr Spectroscopy ◽  
Chemical Properties ◽  
Earth Metal ◽  
Temperature Evolution ◽  
Ir Absorption ◽  
Absorption Bands ◽  
Metal Tungstates

New d-electron and rare-earth metal tungstates (CoRE2W2O10; CoRE4W3O16; Co2RE2W3O14 and NiRE2W2O10) were studied by the IR and EPR spectroscopy methods. The IR absorption bands with their maxima can be assigned to the symmetric and asymmetric stretching modes of W-O bonds in the joint of WO6 octahedra and also to the oxygen double WOOW bridge bonds. The wide, unstructured EPR powder spectra of these compounds and their temperature evolution have been analyzed and interpreted.

Method for determining the formation constants of intermolecular H-bonding from IR spectroscopy data

2021 ◽  
pp. 55-58
Author(s):  
N.U. Mulloev ◽  
◽  
N.L. Lavrik ◽  
J.O. Yusypova ◽  
N.A. Majidov ◽  
...  
Keyword(s):  
Optical Density ◽  
Formation Constants ◽  
Butyl Alcohol ◽  
Proton Donor ◽  
Proton Acceptor ◽  
Ir Absorption ◽  
Visible Spectroscopy ◽  
Absorption Bands ◽  
Intermolecular Hydrogen Bonds ◽  
Uv Visible

An experimental method is proposed for determining the efficiency of the formation of intermolecular hydrogen bonds by determining the formation constant of the H-complex (K). The essence of the experiment to determine the value of K is that for one initial concentration of the proton donor, it is necessary to register the change in the optical density at the absorption wavelength of the monomers and the change in the optical density of the complexes of IR absorption bands at two concentrations of the proton acceptor. This approach was tested on the example of the interaction of butyl alcohol (proton donor) with 4-chloromethyl-1.3-dioxolane (proton acceptor). The obtained value of the equilibrium constant was 72.2 M-1. It is concluded that the proposed method for determining the value of K can be used not only in IR, but also in UV-visible spectroscopy.

Identification of Vibrational Modes in BaSi2 Epitaxial Films by Infrared and Raman Spectroscopy

2018 ◽  
Vol 386 ◽  
pp. 43-47 ◽  
Author(s):  
Hirofumi Hoshida ◽  
Naoki Murakoso ◽  
Takashi Suemasu ◽  
Yoshikazu Terai
Keyword(s):  
Raman Spectroscopy ◽  
Raman Spectra ◽  
Epitaxial Films ◽  
Ir Absorption ◽  
Vibrational Modes ◽  
Depolarization Ratio ◽  
Phonon Line ◽  
Infrared And Raman Spectroscopy ◽  
Raman Intensities ◽  
Polarized Raman

Infrared (IR) absorption and polarized Raman spectra were measured in BaSi2 epitaxial films to investigate the vibrational modes and the symmetry of Si4 cluster in BaSi2. By an analysis based on Raman and/or IR activity in the spectra, the symmetry of Si4 cluster was determined as Th-symmetry and the observed Raman lines and IR peaks were assigned to Ag, Eg, Fg, and Fu, respectively. In the three Raman lines of Fg-mode, one LO phonon line and two TO phonon lines were classified by the depolarization ratio of polarized Raman intensities.

IR spectra of powder hematite: effects of particle size and shape

Clay Minerals ◽  
1981 ◽  
Vol 16 (4) ◽  
pp. 375-382 ◽  
Author(s):  
Jose L. Rendon ◽  
Carlos J. Serna
Keyword(s):  
Particle Size ◽  
Ir Spectra ◽  
Ir Absorption ◽  
Surface Mode ◽  
Absorption Bands ◽  
Size And Shape ◽  
Ir Absorption Spectra ◽  
Theoretical Predictions ◽  
Particle Size And Shape ◽  
Average Size

AbstractHematites obtained by heating goethite gave different IR absorption spectra depending on the temperature of formation. Hematites formed between 250–600°C consisted of lath-like crystals (average size 0.4 ×0.08 µm) and showed, in accordance with theoretical predictions, very similar IR spectra whose absorption bands could all be assigned to surface mode vibrations. However, significantly different IR spectra were given by hematites formed between 700–950°C, the differences being correlated with variations in the size and shape of the particles. Differences observed in the IR spectra of powder hematite do not therefore justify new names for the mineral, as have been proposed in the literature.

scholarly journals OH defect contents in quartz in a granitic system at 1–5 kbar

2019 ◽  
Vol 174 (12) ◽  
Author(s):  
Alexander Potrafke ◽  
Roland Stalder ◽  
Burkhard C. Schmidt ◽  
Thomas Ludwig
Keyword(s):  
Secondary Ion Mass Spectrometry ◽  
Chemical System ◽  
Absorption Feature ◽  
Ir Absorption ◽  
Absorption Bands ◽  
Data Set ◽  
Piston Cylinder ◽  
Oh Defect ◽  
Pressure Interval ◽  
Water Saturated

Abstract Quartz is able to incorporate trace elements (e.g., H, Li, Al, B) depending on the formation conditions (P, T, and chemical system). Consequently, quartz can be used as a tracer for petrogenetic information of silicic plutonic bodies. In this experimental study, we provide the first data set on the OH defect incorporation in quartz from granites over a pressure/temperature range realistic for the emplacement of granitic melts in the upper crust. Piston cylinder and internally heated pressure vessel synthesis experiments were performed in a water-saturated granitic system at 1–5 kbar and 700–950 °C. Crystals from successful runs were analysed by secondary ion mass spectrometry (SIMS) and Fourier transform infrared (FTIR) spectroscopy, and their homogeneity was verified by FTIR imaging. IR absorption bands can be assigned to specific OH defects and analysed qualitatively and quantitatively and reveal that (1) the AlOH band triplet at 3310, 3378 and 3430 cm−1 is the dominating absorption feature in all spectra, (2) no simple trend of total OH defect incorporation with pressure can be observed, (3) the LiOH defect band at 3470–3480 cm−1 increases strongly in a narrow pressure interval from 4 kbar (220 µg/g H2O) to 4.5 kbar (500 µg/g H2O), and declines equally strong towards 5 kbar (180 µg/g H2O). Proton incorporation is charge balanced according to the equation H+ + A+ + P5+ = M3+ + B3+, with A+ = alkali ions and M3+ = trivalent metal ions.

scholarly journals SYNTHESIS AND BIOLOGICAL EVALUATION OF SPIRO (INDOLE-THIAZOLIDINE) DERIVATIVES AS ANTIMICROBIAL AGENTS

2019 ◽  
pp. 71-74
Author(s):  
PRIYANKA NIVRUTTI SHINDE ◽  
MANISH ASHOK RASKAR
Keyword(s):  
Antimicrobial Activity ◽  
Antimicrobial Agents ◽  
Aromatic Aldehydes ◽  
Catalytic Amount ◽  
Biological Evaluation ◽  
Mercaptoacetic Acid ◽  
Ir Absorption ◽  
Absorption Bands ◽  
Synthesis And Biological Evaluation ◽  
Anhydrous Zncl2

Objective: The present study aims to synthesize and biological evaluation of Spiro-[Indole-Thiazolidine] derivatives as antimicrobial agents. Methods: The reaction sequence involves microwave-induced preparation of N-(2-oxo-1,2-dihydro-3’H-indol-3-ylidene)pyridine-4-carbohydrazide [3] from isoniazid [1] and isatin [2] followed by the cyclo condensation of [3] and mercaptoacetic acid under microwave condition to achieve the synthesis of spiro-[indole-thiazolidine] derivatives [4]. The resulting compounds were then allowed to react with various aromatic and heterocyclic aromatic aldehydes to afford arylidene derivatives [5a-l]. Result: Isoniazid (1) on condensation with isatin (2) in the presence of catalytic amount of glacial acetic acid furnished N-(2-oxo-1,2-dihydro-3’H-indol-3-ylidene) pyridine-4-carbohydrazide (3), which showed characteristic IR, absorption bands. Compound (3) underwent Spiro cyclization upon its reaction with mercaptoacetic acid in the presence of anhydrous ZnCl2 to form spiro-[indole-thiazolidine] compound (4). Compound (4) was then condensed with aromatic aldehydes to give arylidene derivatives (5a-l), which were characterized by IR and 1H NMR spectral data. Conclusion: All the synthesized compounds were screened for antimicrobial activity by the cup plate method. Most of the derivatives showed good antimicrobial activity against Gram-Positive and Gram-negative bacteria.

scholarly journals Inclusion Complex of Plai Oil and β-Cyclodextrin

2016 ◽  
Vol 855 ◽  
pp. 47-53
Author(s):  
Ampa Jimtaisong ◽  
Nisakorn Saewan
Keyword(s):  
Inclusion Complex ◽  
Inclusion Complexes ◽  
Physicochemical Characteristic ◽  
Precipitation Method ◽  
Ir Absorption ◽  
Scanning Calorimetry ◽  
Absorption Bands ◽  
Complex Preparation ◽  
Ft Ir ◽  
Co Precipitation

Inclusion complex of β-cyclodextrin (β-CD) and Plai (Zingiber cassumunar) oil was prepared using a simple co-precipitation method at β-CD to Plai oil in different ratios. The inclusion complexes were characterized using Fourier transform-infrared spectroscopy (FT-IR) and differential scanning calorimetry (DSC). The FT-IR absorption bands of inclusion complex at 3600-3200 cm-1 were broader and shifted toward lower frequencies compared with that of pure β-CD (3359 cm-1). DSC of the inclusion complexes showed two endothermic peaks shifted to lower temperatures (90-100°C and 295-300°C) compared to that of β-CD. The different physicochemical characteristic could be an indication of an embedded guest molecule in the β-CD cavities in the inclusion complex preparation.

Sign in / Sign up

Export Citation Format

Share Document