ALUMINA CATALYST: SYNTHESIS OF NOVEL QUINAZOLINE DE RIVATIVES AND THEIR SOLUBILITY INCREASES THROUGH INCLUSION WITH β-CYCLO DEXTRIN (Record no. 11154)

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fixed length control field a
003 - CONTROL NUMBER IDENTIFIER
control field OSt
005 - DATE AND TIME OF LATEST TRANSACTION
control field 20200211094619.0
008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION
fixed length control field 200211b xxu||||| |||| 00| 0 eng d
040 ## - CATALOGING SOURCE
Original cataloging agency AIKTC-KRRC
Transcribing agency AIKTC-KRRC
100 ## - MAIN ENTRY--PERSONAL NAME
9 (RLIN) 12074
Author Hossain, Mossaraf
245 ## - TITLE STATEMENT
Title ALUMINA CATALYST: SYNTHESIS OF NOVEL QUINAZOLINE DE RIVATIVES AND THEIR SOLUBILITY INCREASES THROUGH INCLUSION WITH β-CYCLO DEXTRIN
250 ## - EDITION STATEMENT
Volume, Issue number Vol.11(2)
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 51-58p.
520 ## - SUMMARY, ETC.
Summary, etc. Objective:
To synthesis a novel methodology of bioactive quina
zoline derivatives under greener process to an exce
llent yields and increases their
solubility via inclusion with β-cyclodextrin (CD).
Methods:
Derivatives of quinazoline compounds were prepared
by the mixture of 3-amino-2-phenylquinazolin-4(3H)-
one, derived from 2-phenyl-
4H-benzo[1,3]oxazin-4-one by refluxing with hydrazi
ne, substituted aromatic aldehyde and alumina intim
ately in an agate mortar and pestle under
solvent-free condition. Using various techniques fo
r preparing inclusion complexes, kneaded method is
the best method for encapsulation in host-
guest complex chemistry. All compounds including in
clusion complexes were characterised by spectral me
thods.
Results:
Synthesized a series of novel quinazoline compounds
under a very easier greener process with a commerc
ially available reagent. However,
their low bioavailability, due to low absorption an
d solubility, can limit their potential application
s. CD was used to resolve this solubility problem.
CD can easily accommodated the guest molecules to e
ncapsulate inside its cavity due to interior the hy
drophobic nature with a hydrophilic exterior
part to form thermodynamically more stable molecula
r microcapsules, commonly name as host-guest comple
xes or inclusion complexes. In this
sense, CD was utilized to enhance not only the solu
bility and bioavailability of these quinazoline com
pounds but also their antibacterial capacity.
The formation of inclusion complex was thus confirm
ed by ultraviolet-visible spectroscopy (UV-VIS), Fo
urier Transform Infrared Spectrometry (FT-
IR), differential scanning calorimetry (DSC) and so
lubility study technique.
Conclusion:
Here we have successfully unfolded an eco-friendly
methodology for the synthesis of derivatives of qui
nazoline and increased their
solubility via host-guest inclusion technique. From
the spectral analysis, it was concluded that the q
uinazoline compound is fully encapsulated
inside the cavity of the CD.
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) 12075
Co-Author Nanda, Ashish Kumar
773 0# - HOST ITEM ENTRY
Place, publisher, and date of publication Bhopal Innovare Academic Sciences Pvt Ltd
Title International journal of pharmacy and pharmaceutical science
International Standard Serial Number 2656-0097
856 ## - ELECTRONIC LOCATION AND ACCESS
URL https://innovareacademics.in/journals/index.php/ijpps/article/view/30338/19154
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 2020-02-11 2020888 2020-02-11 2020-02-11 Articles Abstract Database
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