Naproxol
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Naproxol

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Category
Others
Catalog number
BAT-008786
CAS number
26159-36-4
Molecular Formula
C14H16O2
Molecular Weight
216.27
Naproxol
IUPAC Name
(2S)-2-(6-methoxynaphthalen-2-yl)propan-1-ol
Synonyms
(S)-2-(6-methoxynaphthalen-2-yl)propan-1-ol; (S)-(-)-2-(6-Methoxy-2-naphthyl)-1-propanol
Purity
95%
Density
1.108 g/cm3
Boiling Point
362.9ºC at 760 mmHg
InChI
InChI=1S/C14H16O2/c1-10(9-15)11-3-4-13-8-14(16-2)6-5-12(13)7-11/h3-8,10,15H,9H2,1-2H3/t10-/m1/s1
InChI Key
LTRANDSQVZFZDG-SNVBAGLBSA-N
Canonical SMILES
CC(CO)C1=CC2=C(C=C1)C=C(C=C2)OC
1.Impact of chirality on the photoinduced charge transfer in linked systems containing naproxen enantiomers.
Khramtsova EA1, Sosnovsky DV1, Ageeva AA1, Nuin E2, Marin ML2, Purtov PA1, Borisevich SS3, Khursan SL3, Roth HD4, Miranda MA2, Plyusnin VF1, Leshina TV5. Phys Chem Chem Phys. 2016 Apr 21. [Epub ahead of print]
The model reaction of photoinduced donor-acceptor interaction in linked systems (dyads) has been used to study the comparative reactivity of a well-known anti-inflammatory drug, (S)-naproxen (NPX) and its (R)-isomer. (R)- or (S)-NPX in these dyads is linked to (S)-N-methylpyrrolidine (Pyr) using a linear or cyclic amino acid bridge (AA or CyAA), to give (R)-/(S)-NPX-AA-(S)-Pyr flexible and (R)-/(S)-NPX-CyAA-(S)-Pyr rigid dyads. The donor-acceptor interaction is reminiscent of the binding (partial charge transfer, CT) and electron transfer (ET) processes involved in the extensively studied inhibition of the cyclooxygenase enzymes (COXs) by the NPX enantiomers. Besides that, both optical isomers undergo oxidative metabolism by enzymes from the P450 family, which also includes ET. The scheme proposed for the excitation quenching of the (R)- and (S)-NPX excited state in these dyads is based on the joint analysis of the chemically induced dynamic nuclear polarization (CIDNP) and fluorescence data.
2.The Effect of Various Vehicles on the Naproxen Permeability through Rat Skin: A Mechanistic Study by DSC and FT-IR Techniques.
Salimi A1, Hedayatipour N1, Moghimipour E1. Adv Pharm Bull. 2016 Mar;6(1):9-16. doi: 10.15171/apb.2016.003. Epub 2016 Mar 17.
PURPOSE: The purpose of the present investigation was to evaluate the effectiveness of different vehicles on drug permeability and microstructure of intercellular or lipids in SC layer of skin.
3.Preparation and recrystallization behavior of spray-dried co-amorphous naproxen-indomethacin.
Beyer A1, Radi L2, Grohganz H3, Löbmann K4, Rades T5, Leopold CS6. Eur J Pharm Biopharm. 2016 Apr 26. pii: S0939-6411(16)30143-6. doi: 10.1016/j.ejpb.2016.04.019. [Epub ahead of print]
To improve the dissolution properties and the physical stability of amorphous active pharmaceutical ingredients, small molecule stabilizing agents may be added to prepare co-amorphous systems. The objective of the study was to investigate if spray-drying allows the preparation of co-amorphous drug-drug systems such as naproxen-indomethacin and to examine the influence of the process conditions on the resulting initial sample crystallinity and the recrystallization behavior of the drug(s). For this purpose, the process parameters inlet temperature and pump feed rate were varied according to a 22 factorial design and the obtained samples were analyzed with X-ray powder diffractometry and Fourier-transformed infrared spectroscopy. Evaluation of the data revealed that the preparation of fully amorphous samples could be achieved depending on the process conditions. The resulting recrystallization behavior of the samples, such as the total recrystallization rate, the individual recrystallization rates of naproxen and indomethacin as well as the polymorphic form of indomethacin that was formed were influenced by these process conditions.
4.Preparation and characterization of naproxen-loaded electrospun thermoplastic polyurethane nanofibers as a drug delivery system.
Akduman C1, Özgüney I2, Kumbasar EP3. Mater Sci Eng C Mater Biol Appl. 2016 Jul 1;64:383-90. doi: 10.1016/j.msec.2016.04.005. Epub 2016 Apr 4.
The design and production of drug-loaded nanofiber based materials produced by electrospinning is of interest for use in innovative drug delivery systems. In the present study, ultra-fine fiber mats of thermoplastic polyurethane (TPU) containing naproxen (NAP) were successfully prepared by electrospinning from 8 and 10% (w/w) TPU solutions. The amount of NAP in the solutions was 10 and 20% based on the weight of TPU. The collection period of the drug-loaded electrospun TPU fibers was 5, 10 and 20h, and they were characterized by FTIR, DSC and TGA analysis. The morphology of the NAP-loaded electrospun TPU fiber mats was smooth, and the average diameters of these fibers varied between 523.66 and 723.50nm. The release characteristics of these fiber mats were determined by the total immersion method in the phosphate buffer solution at 37°C. It was observed that the collection period in terms of the mat thickness played a major role in the release rate of NAP from the electrospun TPU mats.
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