Myozin Hafif Zincir Kinaz İnhibitörü (ML7) Yüklü Polimerik Nanofiber Formülasyonların Miyometriyum Kasılmasına Etkisi
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Tarih
2023-10-12Yazar
Karasu, Yetkin
Ambargo Süresi
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The aim of this thesis is to design and formulate
a nano-based controllable drug delivery and release system and to investigate its’ in-vitro
effectiveness for preventing premature birth. The effect of nanofibers loaded with calcium
channel blocker (nifedipine) and myosin light chain kinase inhibitor (ML7) on spontaneous
and stimulated myometrial contractions was investigated using uterine tissue obtained from
pregnant women (n= 10) who gave birth by cesarean section at term. Nifedipine and ML7
loaded nanofibers were prepared using the electrospinning method with PLGA polymer. The
prepared polymers were, Group I: Control; Group II: Drug-free nanofiber; Group III:
Nifedipine (10-5
M); Group IV: ML7 (3x10-5 M); Group V: ML7 (3x10-5 M) and Nifedipine (10-5
M); Group VI: ML7 (3x10-5 M) and Nifedipine (3x10-5 M); Group VII: ML7 (3x10-5 M) and
Nifedipine (10-4 M) loaded nanofibers. Nanofibers were applied to the myometrium strips
(3x10 mm) prepared from the term uterine tissue samples and placed in an in-vitro organ
bath. Spontaneous, KCl (120 mM), and cumulative oxytocin (10-11-10-5 M) evoked
contractions were recorded. Contraction amplitudes were normalized by strip weight and
KCl-stimulated contraction, and contraction frequency and area under the curve were
measured. The data were evaluated by the SPSS statistical program. Application of drug loaded polymers resulted in a significant reduction in the frequency and amplitude of the
spontaneous and stimulated contractions in all groups (p<0.01). The results of in the control
and the drug-free nanofiber groups were similar (p=0.704). In terms of amplitude and
frequency of contractions, the most significant effect to the oxytocin dose-contraction
response was recorded in Group VII (p<0.05). In Group VI, the intensity and frequency of
contraction were significantly reduced compared to the control and drug-free nanofiber
groups, as well (p<0.05). These differences became prominent with increasing doses. The use
of Nifedipine or ML7-loaded nanofibers also resulted in decrease in the amplitude and
frequency of contractions, but this decrease was not significant compared to the control and
empty polymer groups. While the maximum contraction response was also significantly
reduced in the drug-applied strips, the most significant difference was observed in Groups VI
and VII (p<0.01). The results of this study show that Nifedipine and ML7-loaded nanofibers
can suppress contractions in human uterine tissue strips. Demonstrating the in vivo
effectiveness of these formulations in further studies will enable locally effective and safe,
controllable drug release systems with reduced systemic side effects to be recommended as
potential treatment options in preterm birth.
Keywords: Preterm birth, Ca2+ channel blocke