Şaşmazel, Hilal Türkoğlu

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S.,Hilal Turkoglu
Sasmazel, Hilal Tuerkoglu
Sasmazel, Hilal Turkoglu
H. T. Şaşmazel
Turkoglu Sasmazel H.
Sasmazel,H.T.
Şaşmazel,H.T.
Hilal Türkoğlu, Şaşmazel
H., Sasmazel
Şasmazel H.
S., Hilal Turkoglu
Ş.,Hilal Türkoğlu
Ş., Hilal Türkoğlu
Turkoğlu Şaşmazel H.
Hilal Turkoglu, Sasmazel
H.T.Sasmazel
H.T.Şaşmazel
Sasmazel H.
Sasmazel, H. T.
Türkoglu, H
Turkoglu, Hilal
Sasmazel, H. Turkoglu
Sasmazel, Hilal T.
H. T. Sasmazel
Şaşmazel, Hilal Türkoğlu
H.,Şaşmazel
Şaşmazel H.
Sasmazel, H. Tuerkodlu
Türkoǧlu Şaşmazel,H.
Şaşmazel, Hilal
Job Title
Profesor Doktor
Email Address
hilal.sasmazel@atilim.edu.tr
Main Affiliation
Metallurgical and Materials Engineering
Status
Website
Scopus Author ID
Turkish CoHE Profile ID
Google Scholar ID
WoS Researcher ID

Sustainable Development Goals

14

LIFE BELOW WATER
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1

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2

ZERO HUNGER
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0

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11

SUSTAINABLE CITIES AND COMMUNITIES
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1

NO POVERTY
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12

RESPONSIBLE CONSUMPTION AND PRODUCTION
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7

AFFORDABLE AND CLEAN ENERGY
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5

GENDER EQUALITY
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3

GOOD HEALTH AND WELL-BEING
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27

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9

INDUSTRY, INNOVATION AND INFRASTRUCTURE
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13

CLIMATE ACTION
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6

CLEAN WATER AND SANITATION
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10

REDUCED INEQUALITIES
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4

QUALITY EDUCATION
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15

LIFE ON LAND
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16

PEACE, JUSTICE AND STRONG INSTITUTIONS
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17

PARTNERSHIPS FOR THE GOALS
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8

DECENT WORK AND ECONOMIC GROWTH
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Documents

45

Citations

1387

h-index

20

Documents

50

Citations

1276

Scholarly Output

55

Articles

38

Views / Downloads

9/0

Supervised MSc Theses

10

Supervised PhD Theses

0

WoS Citation Count

968

Scopus Citation Count

1022

WoS h-index

18

Scopus h-index

18

Patents

0

Projects

0

WoS Citations per Publication

17.60

Scopus Citations per Publication

18.58

Open Access Source

11

Supervised Theses

10

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Journal of Nanoscience and Nanotechnology4
Bio-Medical Materials and Engineering3
International Journal of Biological Macromolecules2
Molecules2
Nanomaterials2
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Now showing 1 - 2 of 2
  • Article
    Citation - WoS: 23
    Citation - Scopus: 25
    Comparison of Cellular Proliferation on Dense and Porous Pcl Scaffolds
    (Ios Press, 2008) Sasmazel, Hilal Tuerkoglu; Gumusderelioglu, Menemse; Gurpinar, Aylin; Onur, Mehmet Ali
    In this contribution, PCL (poly-e caprolactone) scaffolds were prepared by solvent-casting/particle-leaching technique in the presence of two pore formers, PEG(4000) or sucrose molecules in different quantities (0, 10, 20, 30, 40, 50, 55 w/w% PEG(4000)/PCL; 10, 20 w/w% Sucrose/ PCL). The surface and bulk properties of the resulting scaffolds were studied by SEM, DSC and FTIR. SEM photographs showed that, macroporosity was obtained in the PCL structures prepared with sucrose crystals while microporous structure was obtained in the presence of PEG(4000) molecules. Average pore diameters calculated from SEM photographs were 40.1 and 191.2 mu m for 40% PEG(4000)/PCL and 10% Sucrose/PCL scaffolds, respectively. The DSC and FTIR results confirmed that there is no any interaction between pore formers and PCL during structural formation, and both pore formers, PEG(4000) and sucrose, remained independently in the scaffolds. L929 mouse fibroblast cells were seeded onto PCL structures and maintained during 7 days to evaluate cell proliferation. Cell culture results showed that, 10% Sucrose/ PCL scaffold was the most promising substrate for L929 cell growth due to 3-D architecture and macroporous structure of the scaffold.
  • Article
    Citation - WoS: 17
    Citation - Scopus: 19
    Water/O2< Treatment of Pcl Membranes for Biosignal Immobilization
    (Vsp Bv, 2009) Sasmazel, Hilal Tuerkoglu; Manolache, Sorin; Guemuesderelioglu, Menemse
    The main purpose of this study was to obtain COOH functionalities on the surface of poly-epsilon-caprolactone (PCL) membranes using low-pressure water/O-2-plasma-assisted treatment. PCL membranes were prepared using the solvent-casting technique. Then, low-pressure water/O-2 plasma treatments were performed in a cylindrical, capacitively coupled RF-plasma-reactor in three steps: H2O/O-2-plasma treatment; in situ (oxalyl chloride vapors) gas/solid reaction to convert -OH functionalities into -COCl groups; and hydrolysis for final -COOH functionalities. Optimization of plasma modification processes was done using the DoE software program. COOH and OH functionalities on modified surfaces were detected quantitatively using the fluorescent labeling technique and an UVX 300G sensor. Chemical structural information of untreated, plasma treated and oxalyl chloride functionalized PCL membranes were acquired using pyrolysis GC/MS and ESCA analysis. High-resolution AFM images revealed that nanopatterns were more affected than micropatterns by plasma treatments. AFM images recorded with amino-functionalized tips presented increased size of the features on the surface that suggests higher density of the carboxyls on the nanotopographical elements. Low-pressure water/O-2-plasma-treated and oxalyl chloride functionalized samples were biologically activated with insulin and/or heparin biosignal molecules using a PEO (polyoxyethylene bis amine) spacer. The success of the immobilization process was checked qualitatively by ESCA analysis. In addition, fluorescent labeling techniques were used for the quantitative determination of immobilized biomolecules. Cell-culture experiments indicated that biomolecule immobilization onto PCL scaffolds was effective on L929 cell adhesion and proliferation, especially in the presence of heparin. (C) Koninklijke Brill NV, Leiden, 2009