Evaluation of a docetaxel-cisplatin-fluorouracil-Au complex in human oral carcinoma cell line
- 1. King Mongkut's Institute of Technology Ladkrabang
Description
Higher tobacco and alcohol use have led to a consistent increase in head and neck cancer incidence rates. Currently employed chemotherapeutic and surgical treatment are associated with significant drawbacks. Herein, we evaluated the anti-tumour effect of gold nanoparticles as a vehicle for the delivery of a triple chemotherapy drug formulation and elucidated the potential underlying mechanism. The hydrodynamic size of docetaxel, cisplatin, and 5-fluorouracil physically co-adsorbed on Au nanoparticles was 56 ± 0.8 nm, showing a negative zeta potential. Fourier transform infra-red spectroscopy data confirmed that the triple chemotherapy drug successfully interacted with the gold nano-carrier. Au nanoparticles exhibited high loading efficacy of docetaxel (61%), cisplatin (75%), and 5-fluorouracil (90%), with a controlled drug release profile at 24 h. The triple chemotherapy drug formulation was tested in human oral cavity cancer cell line (KB). Cytotoxicity achieved through a synergistic effect between the treatments led to apoptosis, with a lower half-maximal inhibitory concentration indicating higher cytotoxicity than that of plain docetaxel-cisplatin-fluorouracil. Taken together, we demonstrated that the docetaxel-cisplatin-fluorouracil-gold complex exhibited excellent cytotoxicity in KB cells, superior to that docetaxel-cisplatin-fluorouracil.HIGHLIGHTSThe docetaxel-cisplatin-fluorouracil-Au complex showed a controlled drug-release profile at 24 h.The docetaxel-cisplatin-fluorouracil-Au complex exhibited enhanced internalisation efficiency in cells.Au nanoparticles were biocompatible, with no change in apoptosis among cell line.Spherical Au nanoparticles allowed a high volume of incorporated docetaxel, cisplatin, and 5-fluorouracil to steadily attach onto cells.
Translated Descriptions
Translated Description (Arabic)
أدى ارتفاع تعاطي التبغ والكحول إلى زيادة مستمرة في معدلات الإصابة بسرطان الرأس والرقبة. يرتبط العلاج الكيميائي والجراحي المستخدم حاليًا بعيوب كبيرة. هنا، قمنا بتقييم التأثير المضاد للأورام للجسيمات النانوية الذهبية كوسيلة لإيصال تركيبة عقار العلاج الكيميائي الثلاثي وتوضيح الآلية الكامنة المحتملة. كان الحجم الهيدروديناميكي للدوسيتاكسيل والسيسبلاتين و 5 -فلورويوراسيل الممتص فيزيائيًا على جسيمات الاتحاد الافريقي النانوية 56 ± 0.8 نانومتر، مما يدل على إمكانات زيتا سلبية. أكدت بيانات التحليل الطيفي للأشعة تحت الحمراء المحولة من فورييه أن عقار العلاج الكيميائي الثلاثي تفاعل بنجاح مع الناقل النانوي الذهبي. أظهرت جسيمات الاتحاد الافريقي النانوية فعالية تحميل عالية من دوسيتاكسيل (61 ٪)، سيسبلاتين (75 ٪)، و 5 -فلورويوراسيل (90 ٪)، مع لمحة إطلاق المخدرات الخاضعة للرقابة في 24 ساعة. تم اختبار تركيبة عقار العلاج الكيميائي الثلاثي في خط خلايا سرطان تجويف الفم البشري (KB). أدت السمية الخلوية التي تحققت من خلال تأثير تآزري بين العلاجات إلى موت الخلايا المبرمج، مع تركيز مثبط نصف أقصى أقل يشير إلى سمية خلوية أعلى من تركيز دوسيتاكسيل- سيسبلاتين- فلورويوراسيل العادي. أظهرنا معًا أن مركب دوسيتاكسيل- سيسبلاتين- فلورويوراسيل- الذهب أظهر سمية خلوية ممتازة في خلايا KB، متفوقة على ذلك الدوسيتاكسيل- سيسبلاتين- فلورويوراسيل. أضواء عالية أظهر مركب دوسيتاكسيل- سيسبلاتين- فلورويوراسيل- AU ملفًا جانبيًا متحكمًا في إطلاق الدواء في 24 ساعة. أظهر مركب دوسيتاكسيل- سيسبلاتين- فلورويوراسيل- AU كفاءة استيعاب معززة في الخلايا. كانت الجسيمات النانوية متوافقة حيويًا، مع عدم وجود تغيير في الاستماتة بين خط الخلايا. سمحت الجسيمات النانوية الكروية Au بحجم كبير من الدوسيتاكسيل المدمج، والسيسبلاتين، و 5 فلورويوراسيل للالتصاق بثبات على الخلايا.Translated Description (English)
Higher tobacco and alcohol use have led to a consistent increase in head and neck cancer incidence rates. Currently employed chemotherapeutic and surgical treatment are associated with significant drawbacks. Herein, we evaluated the anti-tumour effect of gold nanoparticles as a vehicle for the delivery of a triple chemotherapy drug formulation and elucidated the potential underlying mechanism. The hydrodynamic size of docetaxel, cisplatin, and 5-fluorouracil physically co-adsorbed on Au nanoparticles was 56 ± 0.8 nm, showing a negative zeta potential. Fourier transform infra-red spectroscopy data confirmed that the triple chemotherapy drug successfully interacted with the gold nano-carrier. Au nanoparticles exhibited high loading efficacy of docetaxel (61%), cisplatin (75%), and 5-fluorouracil (90%), with a controlled drug release profile at 24 h. The triple chemotherapy drug formulation was tested in human oral cavity cancer cell line (KB). Cytotoxicity achieved through a synergistic effect between the treatments led to apoptosis, with a lower half-maximal inhibitory concentration indicating higher cytotoxicity than that of plain docetaxel-cisplatin-fluorouracil. Taken together, we demonstrated that the docetaxel-cisplatin-fluorouracil-gold complex exhibited excellent cytotoxicity in KB cells, superior to that docetaxel-cisplatin-fluorouracil.HIGHLIGHTSThe docetaxel-cisplatin-fluorouracil-Au complex showed a controlled drug-release profile at 24 h.The docetaxel-cisplatin-fluorouracil-Au complex exhibited enhanced internalisation efficiency in cells.Au nanoparticles were biocompatible, with no change in apoptosis among cell line.Spherical Au nanoparticles allowed a high volume of incorporated docetaxel, cisplatin, and 5-fluorouracil to steadily attach onto cells.Translated Description (French)
Higher tobacco and alcohol use have led to a consistent increase in head and neck cancer incidence rates. Currently employed chemotherapeutic and surgical treatment are associated with significant drawbacks. Herein, we evaluated the anti-tumour effect of gold nanoparticles as a vehicle for the delivery of a triple chemotherapy drug formulation and élucidated the potential underlying mechanism. The hydrodynamic size of docetaxel, cisplatin, and 5-fluorouracil physically co-adsorbed on Au nanoparticles was 56 ± 0.8 nm, showing a negative zeta potential. Fourier transform infra-red spectroscopy data confirmed that the triple chemotherapy drug successfully interacted with the gold nano-carrier. Au nanoparticles exhibited high loading efficacy of docetaxel (61 %), cisplatine (75 %), and 5-fluorouracil (90 %), with a controlled drug release profile at 24 h. The triple chemotherapy drug formulation was tested in human oral cavity cancer cell line (KB). Cytotoxicity achieved through a synergistic effect between the treatments led to apoptosis, with a lower half-maximal inhibitory concentration indicating higher cytotoxicity than that of plain docetaxel-cisplatin-fluorouracil. Taken together, we demonstrated that the docetaxel-cisplatin-fluorouracil-gold complex exhibited excellent cytotoxicity in KB cells, superior to that docetaxel-cisplatin-fluorouracil.HIGHLIGHTSThe docetaxel-cisplatin-fluorouracil-Au complex showed a controlled drug-release profile at 24 h.The docetaxel-cisplatin-fluorouracil-Au complex exhibited enhanced internalisation efficiency in cells.Au nanoparticles were biocompatible, with no change in apoptosis among cell line.Spherical Au nanoparticles allowed a high volume of incorporated docetaxel, cisplatin, and 5-fluorouracil to steadily attach onto cells.Translated Description (Spanish)
Higher tobacco and alcohol use have led to a consistent increase in head and neck cancer incidence rates. Currently employed chemotherapeutic and surgical treatment are associated with significant drawbacks. Herein, we evaluated the anti-tumour effect of gold nanoparticles as a vehicle for the delivery of a triple chemotherapy drug formulation and elucidated the potential underlying mechanism. The hydrodynamic size of docetaxel, cisplatin, and 5-fluorouracil physically co-adsorbed on Au nanoparticles was 56 ± 0.8 nm, showing a negative zeta potential. Fourier transform infra-red spectroscopy data confirmed that the triple chemotherapy drug successfully interacted with the gold nano-carrier. Au nanoparticles exhibited high loading efficacia of docetaxel (61%), cisplatin (75%), and 5-fluorouracil (90%), with a controlled drug release profile at 24 h. The triple chemotherapy drug formulation was tested in human oral cavity cancer cell line (KB). Cytotoxicity achieved through a synergistic effect between the treatments led to apoptosis, with a lower half-maximal inhibitory concentration indicating higher cytotoxicity than that of plain docetaxel-cisplatin-fluorouracil. Taken together, we demonstrated that the docetaxel-cisplatin-fluorouracil-gold complex exhibited excellent cytotoxicity in KB cells, superior to that docetaxel-cisplatin-fluorouracil.HIGHLIGHTSThe docetaxel-cisplatin-fluorouracil-Au complex showed a controlled drug-release profile at 24 h.The docetaxel-cisplatin-fluorouracil-Au complex exhibited enhanced internalisation efficiency in cells.Au nanoparticles were biocompatible, with no change in apoptosis among cell line.Spherical Au nanoparticles allowed a high volume of incorporated docetaxel, cisplatin, and 5-fluoroura tocil steadily attach onto cells.Additional details
Additional titles
- Translated title (Arabic)
- تقييم مركب دوسيتاكسيل- سيسبلاتين- فلورويوراسيل- أو في سلالة خلايا الورم السرطاني الفموي البشري
- Translated title (English)
- Evaluation of a docetaxel-cisplatin-fluorouracil-Au complex in human oral carcinoma cell line
- Translated title (French)
- Evaluation of a docetaxel-cisplatin-fluorouracil-Au complex in human oral carcinoma cell line
- Translated title (Spanish)
- Evaluation of a docetaxel-cisplatin-fluorouracil-Au complex in human oral carcinoma cell line
Identifiers
- Other
- https://openalex.org/W4360600627
- DOI
- 10.1080/21691401.2023.2189913
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