Kefi Iqbal

Effect of pH, Buffer, and Viscosity on the Photolysis of Formylmethylflavin: A Kinetic Study

The kinetics of the photolysis of formylmethylflavin, a major intermediate product in the aerobic and anaerobic photolysis of riboflavin, was studied in the pH range 2.0–11.0. Formylmethylflavin and its photoproducts, lumichrome and lumiflavin, were determined in degraded solutions using a specific multicomponent spectrophotometric method. The photolysis of formylmethylflavin in alkaline medium takes place by first-order kinetics and the rate constants (kobs) at pH 7.5–11.0 range from 0.27 × 10–4 to 3.88 × 10–4 and 0.36 × 10–4 to 5.63 × 10–4 s–1 under aerobic and anaerobic conditions respectively. In acid medium, the photolysis involves a second-order mechanism and the rate constants at pH 2.0–7.0 range from 1.37 to 2.11 and 2.03 to 2.94 M–1 s–1 under aerobic and anaerobic conditions respectively. The rate–pH profiles for the photolysis reactions indicate the highest rate of formylmethylflavin degradation is at ~pH 4 and above pH 10. In the alkaline region, the increase in rate with pH is due to higher reactivity of the flavin triplet state. The photolysis of formylmethylflavin is catalyzed by phosphate ions and is affected by the solvent viscosity.

Formulation and Stability of Ascorbic Acid in Topical Preparations

Ascorbic acid (vitamin C) and its derivatives are known to perform various important physiological and metabolic functions in humans. In addition to dietary supplements, a number of topical formulations containing ascorbic acid and derivatives are now available that induce collagen synthesis, strengthening of skin tissues, reduction in pigmentation loss, and improved growth and health activities. It has also been used in a variety of cosmetic preparations as an antioxidant, pH adjuster, anti-aging and photoprotecting agent. Ascorbic acid is highly sensitive to air and light; and to achieve its stabilization in cosmetic preparations, it has been suggested to use ascorbic acid in microencapsulation form, in combination with other chemical moieties such as vitamin-E, by the control of pH and electrolyte concentration and use of stabilizing agents like citric, tartaric, or ferulic acids. A large number of cosmetic creams and lotions are available in the market containing the derivatives of ascorbic acid (e.g., sodium ascorbate, ascorbyl palmitate). Although these preparations are chemically stable, they lack the pharmacological activity of ascorbic acid. In the present review, it has been emphasized to consider the importance of various factors involved in the formulation of such preparations to achieve the stabilization of ascorbic acid as such, to maintain its pharmacological activity.

A review of the effect of various ions on the properties and the clinical applications of novel bioactive glasses in medicine and dentistry

Bioactive glass is a novel material that dissolves and forms a bond with bone when exposed to body fluids. Bioactive glasses are silicate-based, with calcium and phosphate in identical proportions to those of natural bone; therefore, they have high biocompatibility. Bioactive glasses have wide-ranging clinical applications, including the use as bone grafts, scaffolds, and coating materials for dental implants. This review will discuss the effects of ions on the various compositions of bioactive glasses, as well as the clinical applications of bioactive glasses in medicine and dentistry.

Photoinitiated Polymerization of 2-Hydroxyethyl Methacrylate by Riboflavin/Triethanolamine in Aqueous Solution: A Kinetic Study

The polymerization of 1–3 M 2-hydroxyethyl methacrylate (HEMA) initiated by riboflavin/triethanolamine system has been studied in the pH range 6.0–9.0. An approximate measure of the kinetics of the reaction during the initial stages (~5% HEMA conversion) has been made to avoid the effect of any variations in the volume of the medium. The concentration of HEMA in polymerized solutions has been determined by a UV spectrophotometric method at 208 nm with a precision of ±3%. The initial rate of polymerization of HEMA follows apparent first-order kinetics and the rates increase with pH. This may be due to the presence of a labile proton on the hydroxyl group of HEMA. The second-order rate constants for the interaction of triethanolamine and HEMA lie in the range of 2.36 to 8.67 × 10−2 M−1 s−1 at pH 6.0–9.0 suggesting an increased activity with pH. An increase in the viscosity of HEMA solutions from 1 M to 3 M leads to a decrease in the rate of polymerization probably as a result of the decrease in the reactivity of the flavin triplet state. The effect of pH and viscosity of the medium on the rate of reaction has been evaluated.

Correction for Irrelevant Absorption in Multicomponent Spectrophotometric Assay of Riboflavin, Formylmethylflavin, and Degradation Products: Kinetic Applications

In the spectrophotometric assay of multicomponent systems involved in drug degradation studies, some minor or unknown degradation products may be present. These products may interfere in the assay and thus invalidate the results due to their absorption in the range of analytical wavelengths. This interference may be eliminated by the application of an appropriate correction procedure to obtain reliable data for kinetic treatment. The present study is based on the application of linear and non-linear irrelevant absorption corrections in the multicomponent spectrophotometric assay of riboflavin and formylmethylflavin during the photolysis and hydrolysis studies. The correction procedures take into account the interference caused by minor or unknown products and have shown considerable improvement in the assay data in terms of the molar balance. The treatment of the corrected data has led to more accurate kinetic results in degradation studies.

Chemical and morphological characteristics of mineral trioxide aggregate and Portland cements

The purpose of this study was to investigate the chemical composition and particle morphology of white mineral trioxide aggregate (WMTA) and two white Portland cements (CEM 1 and CEM 2). Compositional analysis was performed by energy dispersive X-ray spectroscopy, X-ray fluorescence spectrometry and X-ray diffraction whereas, morphological characteristics were analyzed by scanning electron microscope and Laser scattering particle size distribution analyzer. The elemental composition of WMTA, CEM 1 and CEM 2 were similar except for the presence of higher amounts of bismuth in WMTA. Calcium oxide and silicon oxide constitute the major portion of the three materials whereas, tricalcium silicate was detected as the major mineral phase. The particle size distribution and morphology of WMTA was finer compared to CEM 1 and CEM 2. The three tested materials had relatively similar chemical composition and irregular particle morphologies.

Solvent Effect on Photoinitiator Reactivity in the Polymerization of 2-Hydroxyethyl Methacrylate

Efficacy of photoinitiators such as riboflavin (RF), camphorquinone (CQ), and safranin T (ST) and triethanolamine as a coinitiator has been compared in carrying out the polymerization of 2-hydroxyethyl methacrylate (HEMA) in aqueous and organic solvents. HEMA solutions were polymerized in the presence of RF, CQ, and ST using a low intensity visible radiation source. HEMA was assayed by a UV spectrophotometric method during the initial stages of the reactions (i.e., ~5% change). A comparison of the efficacy of photoinitiators in causing HEMA polymerization showed that RF is more efficient than CQ and ST. The rate of polymerization is directly related to solvent dielectric constant and inversely related to the solvent viscosity. RF is the most efficient photoinitiator in the polymerization of HEMA and the highest rate of reaction occurs in aqueous solutions. A general scheme for the polymerization of HEMA in the presence of photoinitiators is presented.