EFFECT OF LOVASTATIN NANO DRUG DELIVERY SYSTEM ON B ONE MINERAL DENSITY (BMD) AND BIOMECHANICAL PROPERTIES OF TIBIA BONES O F WISTAR RATS (Record no. 11132)

000 -LEADER
fixed length control field a
003 - CONTROL NUMBER IDENTIFIER
control field OSt
005 - DATE AND TIME OF LATEST TRANSACTION
control field 20200210103740.0
008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION
fixed length control field 200210b xxu||||| |||| 00| 0 eng d
040 ## - CATALOGING SOURCE
Original cataloging agency AIKTC-KRRC
Transcribing agency AIKTC-KRRC
100 ## - MAIN ENTRY--PERSONAL NAME
9 (RLIN) 12041
Author Kaur, Ramandeep
245 ## - TITLE STATEMENT
Title EFFECT OF LOVASTATIN NANO DRUG DELIVERY SYSTEM ON B ONE MINERAL DENSITY (BMD) AND BIOMECHANICAL PROPERTIES OF TIBIA BONES O F WISTAR RATS
250 ## - EDITION STATEMENT
Volume, Issue number Vol.11(9)
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 42-48p.
520 ## - SUMMARY, ETC.
Summary, etc. Objective:
In the present study, transdermal nanoemulsion (NE)
gel of lovastatin was investigated for its anti-os
teoporosis effect on the long bones
of rat i.e. tibia.
Methods:
Male wistar rats (n=30, weighing 180-200g) were tak
en for this study and grouped as: 1) control (norma
l saline daily), 2) Dex
(dexamethasone sodium; 25 mg/kg subcutaneously twic
e a week), 3) Dex+LNG5 (lovastatin nanoemulsion gel
; 5 mg/kg/d transdermally daily), 4)
Dex+LNG10 (lovastatin nanoemulsion gel; 10 mg/kg/d
transdermally daily), and 5) Dex+ALN (alendronate s
odium; 0.03 mg/kg/d orally daily). All
the treatments were carried out for 60 d. At the en
d of the experiment, all animals were anesthetized
using diethyl ether and collected blood
samples from retro-orbital venous plexus of rats in
dry eppendorf tubes followed by the sacrifice of a
nimals by cervical dislocation method and
collected tibia bones of both the legs for analysis
.
Results:
Bone formation biomarkers (OC: osteocalcin, b-ALP:
bone-specific alkaline phosphatase, PINP: N-termina
l propeptides of type I procollagen)
were significantly improved and resorption biomarke
rs (CTx: C-terminal cross-linking telopeptides of t
ype-I collagen, TRAcP5b: isoform 5b of tartarate
resistant acid phosphatase) were significantly redu
ced in the LNG5 (p<0.05) and LNG10 (p<0.05) treatme
nt groups when compared to Dex.
In vivo
anti-
osteoporotic results demonstrated the formation of
new bone in osteoporotic rat tibias. Biomechanical
strength testing demonstrated increased load-
bearing capacity of rat tibias in the treated anima
ls in comparison with the osteoporotic group (p<0.0
5 for LNG5 and p<0.01 for LNG10).
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) 9738
Co-Author Ajitha, Makula
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/34624/20639
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 2020-02-10 2020872 2020-02-10 2020-02-10 Articles Abstract Database
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