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1.
J Pharm Sci ; 104(12): 4355-4364, 2015 Dec.
Article in English | MEDLINE | ID: mdl-26523412

ABSTRACT

The oxidation reaction of pyridine by hydrogen peroxides in water media was investigated by combining quantum chemical calculations and laboratory experiments. Pyridine was selected as a model system for aromatic amines that frequently occurs in drug molecules. Several different reaction conditions, commonly used in stress testing of drug molecules during drug development, were investigated to increase mechanistic insight to this class of oxidation reactions. Of special interest is to note that small amounts of acetonitrile, a regularly used cosolvent to keep poorly soluble drug molecules in water solution, could catalyze the oxidation reaction in the presence of hydrogen peroxide. Consequently, attention needs to be taken when comparing data from different stress test studies of amine oxidation by hydrogen peroxides at different pH, and with and without acetonitrile. In particular, they need to be controlled when identifying the proper intrinsic stability of the drug molecule.


Subject(s)
Pyridines/chemistry , Acetonitriles/chemistry , Amines/chemistry , Catalysis , Hydrogen Peroxide/chemistry , Hydrogen-Ion Concentration , Oxidation-Reduction , Water/chemistry
2.
J Pharm Sci ; 104(4): 1409-20, 2015 Apr.
Article in English | MEDLINE | ID: mdl-25712623

ABSTRACT

We have developed a predictive method, based on quantum chemical calculations, that qualitatively predicts N-oxidation by hydrogen peroxides in drug structures. The method uses linear correlations of two complementary approaches to estimate the activation barrier without calculating it explicitly. This method can therefore be automated as it avoids demanding transition state calculations. As such, it may be used by chemists without experience in molecular modeling and provide additional understanding to experimental findings. The predictive method gives relative rates for N,N-dimethylbenzylamine and N-methylmorpholine in good agreement with experiments. In water, the experimental rate constants show that N,N-dimethylbenzylamine is oxidized three times faster than N-methylmorpholine and in methanol it is two times faster. The method suggests it to be two and five times faster, respectively. The method was also used to correlate experimental with predicted activation barriers, linear free-energy relationships, for a test set of tertiary amines. A correlation coefficient R(2) = 0.74 was obtained, where internal diagnostics in the method itself allowed identification of outliers. The method was applied to four drugs: caffeine, azelastine, buspirone, and clomipramine, all possessing several nitrogens. Both overall susceptibility and selectivity of oxidation were predicted, and verified by experiments.


Subject(s)
Amines/chemistry , Computer Simulation , Hydrogen Peroxide/chemistry , Methanol/chemistry , Models, Chemical , Solvents/chemistry , Water/chemistry , Chemistry, Pharmaceutical , Drug Storage , Kinetics , Linear Models , Oxidation-Reduction , Reproducibility of Results , Technology, Pharmaceutical/methods , Time Factors
3.
Chem Res Toxicol ; 24(9): 1507-15, 2011 Sep 19.
Article in English | MEDLINE | ID: mdl-21823635

ABSTRACT

The autoxidation of geranial with O(2) was studied both experimentally and using density functional theory. Computational results were used to interpret experimentally observed product ratios. Geranial was found to autoxidize, forming 6,7-epoxygeranial as the main oxidation product. Hydroperoxides corresponding to those identified as important skin sensitizers in previous studies of fragrance terpenes could not be detected. Instead, a dioxolan derivative and its corresponding hydroperoxide were identified and detected in high concentrations. The distribution of products in autoxidation generally depends on the stabilities of the intermediate peroxyl radicals. In this study, the formation of a peracyl radical was found to be highly favored. This radical forms peracid which epoxidizes geranial. The epoxide thus produced can react with acyl radical to yield the dioxolan hydroperoxide. The dioxolan derivative is believed to form in an acid catalyzed closed shell reaction between 6,7-epoxygeranial and geranial. The dioxolan hydroperoxide and 6,7-epoxygeranial are strong sensitizers and are considered to be the compounds mainly responsible for the skin sensitization potency of air-exposed geranial.


Subject(s)
Allergens/chemistry , Dermatitis, Allergic Contact/etiology , Dioxolanes/chemistry , Hydrogen Peroxide/chemistry , Monoterpenes/chemistry , Acyclic Monoterpenes , Allergens/adverse effects , Animals , Dioxolanes/adverse effects , Hydrogen Peroxide/adverse effects , Local Lymph Node Assay , Mice , Monoterpenes/adverse effects , Oxidation-Reduction , Skin/drug effects
4.
Dalton Trans ; 40(42): 11308-14, 2011 Nov 14.
Article in English | MEDLINE | ID: mdl-21738934

ABSTRACT

The two distinct mechanistic pathways of the Heck reaction, cationic and neutral, are characterized computationally using DFT calculations with corrections for solvation and dispersion. The selectivity in each type of reaction is discussed in terms of the detailed reaction paths, and the two types are compared to each other. The geometries and energies of the selectivity-determining transitions states are analyzed in detail.


Subject(s)
Alkenes/chemistry , Palladium/chemistry , Quantum Theory , Ammonia/chemistry , Chlorides/chemistry , Kinetics , Ligands , Organophosphorus Compounds/chemistry , Oxidation-Reduction , Thermodynamics
5.
Chemistry ; 14(31): 9549-54, 2008.
Article in English | MEDLINE | ID: mdl-18785678

ABSTRACT

Pathways for formation of previously observed autoxidation products of ethoxylated surfactants have been studied by DFT (B3LYP). In addition to the established radical-chain reaction, several mechanistic possibilities for intramolecular fragmentation of the intermediate radicals have been characterized concerning reaction barriers and energies of transition states. The results can rationalize the formation of previously observed autoxidation products, including several, which have been implicated as strongly allergenic.


Subject(s)
Air , Ethyl Ethers/chemistry , Surface-Active Agents/chemistry , Alcohols/chemistry , Computers , Free Radicals/chemistry , Hydrogen/chemistry , Molecular Structure , Oxidation-Reduction , Peroxides/chemistry
6.
J Chem Theory Comput ; 4(1): 101-6, 2008 Jan.
Article in English | MEDLINE | ID: mdl-26619983

ABSTRACT

The fragrance terpene geraniol autoxidizes upon air exposure and forms a mixture of oxidation products, some of which are skin sensitizers. Reactions of geraniol with O2 have been studied with DFT (B3LYP) and the computational results compared to experimentally observed product ratios. The oxidation is initiated by hydrogen abstraction, forming an allylic radical which combines with an O2 molecule to yield an intermediate peroxyl radical. In the subsequent step, geraniol differs from previously studied cases, in which the radical chain reaction is propagated through intermolecular hydrogen abstraction. The hydroxy-substituted allylic peroxyl radical prefers an intramolecular rearrangement, producing observable aldehydes and the hydroperoxyl radical, which in turn can propagate the radical reaction. Secondary oxidation products like epoxides and formates were also considered, and plausible reaction pathways for formation are proposed.

7.
Chem Res Toxicol ; 20(5): 807-14, 2007 May.
Article in English | MEDLINE | ID: mdl-17428070

ABSTRACT

Fragrances are common causes of contact allergy. Geraniol (trans-3,7-dimethyl-2,6-octadiene-1-ol) is an important fragrance terpene. It is considered a weak contact allergen and is used for fragrance allergy screening among consecutive dermatitis patients. Analogous to other monoterpenes studied, such as limonene and linalool, geraniol has the potential to autoxidize on air exposure and form highly allergenic compounds. The aim of the present study was to investigate and propose a mechanism for the autoxidation of geraniol at room temperature. To investigate whether allergenic compounds are formed, the sensitizing potency of geraniol itself, air-exposed geraniol, and its oxidation products was determined using the local lymph node assay in mice. The results obtained show that the allylic alcohol geraniol follows an oxidation pattern different from those of linalool and limonene, which autoxidize forming hydroperoxides as the only primary oxidation products. The autoxidation of geraniol follows two paths, originating from allylic hydrogen abstraction near the two double bonds. From geraniol, hydrogen peroxide is primarily formed together with aldehydes geranial and neral from a hydroxyhydroperoxide. In addition, small amounts of a hydroperoxide are formed, analogous to the formation of the major linalool hydroperoxide. The autoxidation of geraniol greatly influenced the sensitizing effect of geraniol. The oxidized samples had moderate sensitizing capacity, quite different from that of pure geraniol. The hydroperoxide formed is believed to be the major contributor to allergenic activity, together with the aldehydes geranial and neral. On the basis of the present study and previous experience, we recommend that the possibility of autoxidation and the subsequent formation of contact allergenic oxidation products are considered in risk assessments performed on fragrance terpenes.


Subject(s)
Allergens/chemistry , Dermatitis, Allergic Contact/etiology , Perfume/chemistry , Perfume/toxicity , Terpenes/chemistry , Terpenes/toxicity , Acyclic Monoterpenes , Air , Allergens/toxicity , Animals , Dermatitis, Allergic Contact/pathology , Hydrogen Peroxide/analysis , Hydrogen Peroxide/toxicity , Immunization , Local Lymph Node Assay , Lymph Nodes/drug effects , Lymph Nodes/metabolism , Lymph Nodes/pathology , Mice , Oxidation-Reduction
8.
J Phys Chem A ; 110(44): 12204-12, 2006 Nov 09.
Article in English | MEDLINE | ID: mdl-17078616

ABSTRACT

This study concerns the autoxidation of one of the most used fragrances in daily life, linalool (3,7-dimethyl-1,6-octadien-3-ol). It reacts with O2 to form hydroperoxides, which are known to be important contact allergens. Pathways for hydroperoxide formation are investigated by means of quantum mechanical electronic structure calculations. Optimized molecular geometries and harmonic vibrational frequencies are determined using density functional theory (DFT). Insight into how the addition of O2 to linalool occurs is obtained by establishing a theoretical framework and systematically investigating three smaller systems: propene, 2-methyl-2-butene, and 2-methyl-2-pentene. 2-Methyl-2-pentene was chosen as a model system and used to compare with linalool. This theoretical study characterizes the linalool-O2 biradical intermediate state, which constitutes a branching point for the further oxidation reactions pathways. Thus, the observed linalool oxidation product spectrum is discussed in terms of a direct reaction path, the ene-type mechanism, and the radical mechanism. The major hydroperoxide found in experiments is 7-hydroperoxy-3,7-dimethyl-octa-1,5-diene-3-ol, and the calculated results support this finding.


Subject(s)
Alkenes/chemistry , Fatty Alcohols/chemistry , Monoterpenes/chemistry , Quantum Theory , Acyclic Monoterpenes , Computer Simulation , Free Radicals/chemistry , Insecticides/chemistry , Models, Chemical , Molecular Structure , Oxidation-Reduction
9.
Contact Dermatitis ; 55(4): 230-7, 2006 Oct.
Article in English | MEDLINE | ID: mdl-16958922

ABSTRACT

Concomitant positive reactions to colophonium, oxidized limonene, and/or oxidized linalool are recorded in patch test studies. The main allergens in these patch test mixtures are hydroperoxides, which form antigens by a radical pathway. Theoretically, concomitant reactions can be explained not only by concomitant sensitization or by true cross-reactions but also by the hydroperoxides acting as oxidizing agents on skin proteins to form non-specific antigens without hapten-protein binding. The aim of this study was to explore concomitant reactions and cross-reactivity patterns among hydroperoxide haptens. We investigated whether individuals allergic to the main allergen in colophonium, 15-hydroperoxyabietic acid, would also react to limonene hydroperoxide or linalool hydroperoxide. Only 1 of 29 individuals reacted to more than 1 hydroperoxide. The cross-reactivity pattern among cumene hydroperoxide, limonene hydroperoxide, 1-(1-hydroperoxy-1-methylethyl) cyclohexene (cyclohexene hydroperoxide), and 15-hydroperoxydehydroabietic acid was investigated in guinea-pigs. No general cross-reactivity was observed. Cross-reactions between cumene hydroperoxide and cyclohexene hydroperoxide show that similarity in the overall structure and the way of antigen formation are needed. Quantum calculations were used to determine the formation energies of the intermediary radicals. We concluded that hydroperoxides form specific antigens and that formation of non-specific antigens is unlikely. The concomitant patch test reactions described in the literature are best explained as a result of multiple sensitizations.


Subject(s)
Allergens/chemistry , Dermatitis, Allergic Contact/etiology , Hydrogen Peroxide/chemistry , Allergens/adverse effects , Allergens/immunology , Animals , Antigens/biosynthesis , Benzene Derivatives/chemistry , Cross Reactions , Cyclohexenes/chemistry , Female , Guinea Pigs , Humans , Hydrogen Peroxide/adverse effects , Hydrogen Peroxide/immunology , Limonene , Male , Middle Aged , Patch Tests , Terpenes/chemistry
10.
J Phys Chem A ; 109(14): 3105-10, 2005 Apr 14.
Article in English | MEDLINE | ID: mdl-16833636

ABSTRACT

Car-Parrinello molecular dynamics (CPMD) and a previously developed wave packet model are used to study ultrafast relaxation in water clusters. Water clusters of 15 water molecules are used to represent ice Ih. The relaxation is studied by exciting a symmetric or an asymmetric stretch mode of the central water molecule. The CPMD results suggest that relaxation occurs within 100 fs. This is in agreement with experimental work by Woutersen and Bakker and the earlier wave packet calculations. The CPMD results further indicate that the excitation energy is transferred both intramolecularly and intermolecularly on roughly the same time scale. The intramolecular energy transfer occurs predominantly between the symmetric and asymmetric modes while the bend mode is largely left unexcited on the short time scale studied here.

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