IMPROVEMENT OF BETULIN-3, 28-DIPHOSPHATE WATER- SOLUBILITY BY COMPLEXATION WITH AMINES–MEGLUMINE AND XYMEDON (Record no. 11194)

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003 - CONTROL NUMBER IDENTIFIER
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005 - DATE AND TIME OF LATEST TRANSACTION
control field 20200212134542.0
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fixed length control field 200212b xxu||||| |||| 00| 0 eng d
040 ## - CATALOGING SOURCE
Original cataloging agency AIKTC-KRRC
Transcribing agency AIKTC-KRRC
100 ## - MAIN ENTRY--PERSONAL NAME
9 (RLIN) 12148
Author Melnikova, Nina
245 ## - TITLE STATEMENT
Title IMPROVEMENT OF BETULIN-3, 28-DIPHOSPHATE WATER- SOLUBILITY BY COMPLEXATION WITH AMINES–MEGLUMINE AND XYMEDON
250 ## - EDITION STATEMENT
Volume, Issue number Vol.11(5)
260 ## - PUBLICATION, DISTRIBUTION, ETC.
Place of publication, distribution, etc. M P
Name of publisher, distributor, etc. Innovare Academic Sciences Pvt Ltd
Year 2019
300 ## - PHYSICAL DESCRIPTION
Pagination 48-55p.
520 ## - SUMMARY, ETC.
Summary, etc. Objective:
To study betulin-3,28-diphosphate (BDP) water solub
ility improved by forming salt complexes with hydro
philic amino alcohols:
meglumine as acidosis corrector and xymedon as the
water-soluble antioxidant.
Methods:
We used
13
C-,
31
P-NMR, UV-spectroscopy and potentiometric titration
to study the BDP-amine salt complexes formation an
d their
solubility using HPLC-analysis.
Results:
The participation of xymedon in the proton transfer
reaction with BDP in aqueous solutions was confirm
ed by the bathochromic shift of
the carbonyl band from 299.1 nm to 304.2 nm, and by
a hyperchromic effect (molar extinction ε from 850
8 to 10 441 l·mol
-1
·cm
-1
) in UV-spectra.
BDP complexation with meglumine was estimated by UV
-spectral molar ratio method at 256 nm. Molar ratio
of BDP-amine complexes (1:4) was
proved by
31
P-NMR. The chemical shift of phosphorus at C-3 atom
of BDP (δ =-0.58 ppm) changed to+3.39 ppm, and at
C-28 atom (δ =+0.28 ppm)–
to+4.60 ppm. BDP solubility increased 100-600 fold
according to HPLC-analysis.
Conclusion:
BDP interaction with amine in an aqueous solution w
as shown to proceed via a proton transfer due to re
latively weak forces such as
London forces, hydrogen bonding, electrostatic and
hydrophobic interactions. In general, the formation
of BDP salt complexes with amines in
solution determines BDP water solubility. Water-sol
uble BDP enables to develop hydrophilic dosage form
s.
650 #0 - SUBJECT ADDED ENTRY--TOPICAL TERM
9 (RLIN) 4639
Topical term or geographic name entry element PHARMACEUTICS
700 ## - ADDED ENTRY--PERSONAL NAME
9 (RLIN) 12149
Co-Author Malygina, Darina
773 0# - HOST ITEM ENTRY
International Standard Serial Number 2656-0097
Title International journal of pharmacy and pharmaceutical science
Place, publisher, and date of publication Bhopal Innovare Academic Sciences Pvt Ltd
856 ## - ELECTRONIC LOCATION AND ACCESS
URL https://innovareacademics.in/journals/index.php/ijpps/article/view/32707/19864
Link text Click here
942 ## - ADDED ENTRY ELEMENTS (KOHA)
Source of classification or shelving scheme
Koha item type Articles Abstract Database
Holdings
Withdrawn status Lost status Source of classification or shelving scheme Damaged status Not for loan Permanent Location Current Location Shelving location Date acquired Barcode Date last seen Price effective from Koha item type
          School of Pharmacy School of Pharmacy Archieval Section 2020-02-12 2020927 2020-02-12 2020-02-12 Articles Abstract Database
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