2. INTRODUCTION- antitumoral drugs
Platinum drugs
low molecular weight alkylating drug
cytotoxic effect: inhibition of DNA synthesis. intercalates into the double helix of
DNA and establishes intra and intercatenary bonds
stops the cell cycle in the G2 phase and activates apoptosis
Nephrotoxicity: directly induces necrosis and apoptosis of tubular kidney cells
3. DELIVERY SYSTEMS DRUGS
biocompatible polymeric materials
Lycium barbarum polysaccharide
fruit of the goji berry (Solanaceae)
LBP: extracellular signal-regulated kinase which in turn affects p53 expression
regulating tumor apoptosis induce cell cycle arrest
of a variety of cancer cells at G0/G1, S, or G2/M phase
5. MATERIALES Y METODOS
PANC-1 (human pancreatic cancer)
MCF-7 (human breast cancer)
293A (human normal kidney)
A549 (human lung cancer cell line)
las células se probaron midiendo la mitad
inhibidor máximo de concentración (IC50)
6. SINTESIS DEL CONJUGADO LBP-5-ASA
Los conjugados LBP-5-ASA se sintetizaron a través de la base de Schiff reacción
entre LBP-CHO y 5-ASA
el grupo aldehído de LBP oxidada reaccionó con el grupo amino del ácido 5-
aminosalicílico (5-ASA) para formar la base de Schiff.
5-ASA se usó para coordinar complejos de Pt con el fin de construir nuevos
fármacos de Polisacáridos (conjugados LBP-5ASA-Pt),
7. CITOTOXICIDAD
Las citotoxicidades de los conjugados LBP, LBP-5-ASA y LBP-5-ASA-Pt
fueron expresados por la concentración de inhibición (IC50).
Las células PANC-1, MCF-7, A549 y 293A se utilizaron para estudiar el potencial
terapéutico de LBP-5-ASA-Pt se conjuga como material terapéutico tumoral in
vitro.
8. ELECTROFORESIS
se llevó a cabo para investigar la interacción de
los conjugados LBP, 5-ASA-Pt con ADN
Finalmente, los resultados de la incubación. de
electroforesis en gel de agarosa
ADN se incubó con conjugados LBP-5-ASA-Pt
durante 24 ha diferentes concentraciones.
9. CITOMETRIA DE FLUJO
Se analizó el contenido de ADN de las
células para estudiar el ciclo celular.
distribución de fases de células A549 en
respuesta a los conjugados LBP-5-ASA-Pt
Fueron tratados con Rnase
Se obtuvieron un total de 10,000 eventos
y el porcentaje de células en cada etapa
se determinó haciendo referencia a
células no tratadas
12. Interaction of LBP-5-ASA-Pt conjugates with
DNA
DNA negative to
positive electrodes
the mobility of DNA is
slightly delayed
damage induced upon
binding of LBP-5-ASA-
Pt conjugates to DNA
interferes with normal
transcription and/or
DNA replication
lead to cell death
Lane 3: 3.6 μM;
13. Fluorescent image
LBP-5-ASA-Pt conjugates
for 48 h at the different
concentrations, nuclei
containing condensed
chromatin obviously
increased, suggesting that
apoptosis of A549 cells was
significantly induced
14. DISCUSSION Author mentioned was mentioned
J. Qiu The effects of LBP, LBP-5-
ASA and LBP-5-ASA-Pt
conjugates, 5-ASA,
oxaliplatin and ASA-Pt
complex on cell viability
were tested using the
MTT assay
K.J. Haxton Pt was bonded with LBP-
5- ASA including has -
COOH and -OH as the
leaving group of platinum
drugs
A.V. Nascimento and S.
O’Grady
Pt as a crosslinking agent,
binds to DNA to form Pt-
DNA adducts resulting in
irreversible lesions in the
double helix and ultimate
cell death
15. conclusions
1. it was evident that the use of different concentrations of the conjugate gave
good results regarding the induction of apoptosis in certain types of cancer
different variables must be found in order to explain why the conjugate had an
effect on certain cells such as the use of conjugates with platinum gave better
results