Araştırma Makalesi
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Yardımcı Maddelerin İlaç Formülasyonundaki Etkilerini Araştırmak İçin In vitro Testler

Yıl 2023, , 292 - 299, 15.08.2023
https://doi.org/10.22312/sdusbed.1328230

Öz

İlaçların formülasyonu, farmakolojik olarak aktif kabul edilmeyen ve bir ilaç formülasyonunda farklı rollere sahip olabilecek bazı eksipiyanlarla birleştirilebilen aktif farmasötik bileşenler (API) gerektirir. Bir biguanid antidiyabetik olarak jenerik bir isim olan Glukofen, diyet yönetimi ve egzersiz yeterli glisemik kontrole yardımcı olmadığında, özellikle aşırı kilolu hastalarda tip 2 Diabetes Mellitus tedavisinde kullanılır. Glukofen formülasyonunda, bir API olarak metformin-HCl ve povidon, magnezyum stearat, hipromelloz ve titanyum dioksit gibi bazı yardımcı maddeler birleştirilir. Bu çalışmanın amacı, Glukofen ve metformin-HCl'nin insan bronşiyal epitel hücre dizisi (Beas-2b) üzerindeki etkilerinin in vitro araştırılmasıdır. Toksik etkilerini ve hücrelere alımlarını gözlemlemek ve karşılaştırmak için sitotoksisite testi ve akış sitometrisi deneyleri yapıldı. Bu çalışmadan elde edilen sonuçlar, hem Glukofen hem de metformin-HCl'nin Beas-2b hücreleri üzerinde herhangi bir toksik etkisinin elde edilmediğini göstermiştir. Ayrıca Glukofen'in hücrelere alımı, metformin-HCl'den daha fazla gözlendi. Yardımcı maddelerin metformin-HCl'ye dahil edilmesinin, hücre çoğalmasında ve hücrelere alınmasında önemli bir artışa yol açtığı açıktır.

Kaynakça

  • [1] Katny, M., Frankowski, M. 2016. Impurities in Drug Products and Active Pharmaceutical Ingredients. Critical Reviews in Analytical Chemistry, 47 (3), 187-193
  • [2] Jain, D., Basniwal, P. 2013. Forced degradation and impurity profiling: Recent trends in analytical perspectives. Journal of Pharmaceutical and Biomedical Analysis, 86, 11-35.
  • [3] Bardal, S., Waechter, J., Martin, D. 2011. Pharmacokinetics. In S. Bardal, J. Waechter, D. Martin, Applied Pharmacology (pp. 17-34). St. Louis, Missouri: Elsevier Saunders.
  • [4] Fortunak, J. M., de Souza, R. O., Kulkarni, A. A., King, C. L., Ellison, T., Miranda, L. S. 2014. Active pharmaceutical ingredients for antiretroviral treatment in low- and middle-income countries: a survey. Antiviral Therapy, 15-29.
  • [5] Fabiano, V., Mameli, C., Zuccotti, G. 2011. Pediatric Pharmacology: Remember the excipients. Pharmacological Research, 63 (5), 362-365.
  • [6] Hamman, J., Steenekamp, J. 2011. Excipients with specialized functions for effective drug delivery. Expert Opinion on Drug Delivery, 9 (2), 219-230.
  • [7] Çubuk, G., İnce, S. 2015. Oral Antidiyabetik İlaçlar. Kocatepe Veteriner Dergisi, 95-102.
  • [8] Li, C., Martini, L., Ford, J., & Roberts, M. 2005. The use of hypromellose in oral drug delivery. Journal of Pharmacy and Pharmacology, 57 (5), 533-546.
  • [9] Rowe, R. 1984. Materials used in the film coating of oral dosage forms. Critical Reports on Applied Chemistry, 6, 1-36.
  • [10] Adeyeye, C., Barabas, E. 1993. Excipient Profile: Povidone. In H. G. Brittain (Ed.), Analytical Profiles of Drug Substances and Excipients (Vol. 22, pp. 555-585). London: Academic Press.
  • [11] Butcher, A., Jones, T. 1972. Some physical characteristics of magnesium stearate. The Journal of Pharmacy and Pharmacology, 1P-9P.
  • [12] Lerk, C., Bolhuis, G., Smallenbroek, A., Zuurman, K. 1982. Interaction of tablet disintegrants and magnesium stearate during mixing. II. Effect on dissolution rate. Pharmaceutica acta Helvetiae, 282-286.
  • [13] Yen, FS., Wei, J.CC., Yang, YC. 2020. Respiratory outcomes of metformin use in patients with type 2 diabetes and chronic obstructive pulmonary disease. Scientific Reports, 10, 10298.
  • [14] Hinge, M A., Patel, KV. 2016. Development and Validation of Spectrophotometric Method for Metformin and Sitagliptin by Absorbance Ratio Method. J Pharm Sci Bioscientific Res. 6(5): 733-739.
  • [15] Holley, R. W. 1975. Control of growth of mammalian cells in cell culture. Nature, 487-490.
  • [16] Hansel, C., Barr, S., Schemann, A.V., Lauber, K., Hess, J., Unger, K., Zitzelsberger, H., Jendrossek, V., Klein, D. 2021. Metformin Protects against Radiation-Induced Acute Effects by Limiting Senescence of Bronchial-Epithelial Cells. International Journal of Science. 22, 7064.
  • [17] Pandey, P., Balekar, N. 2018. Target-specific Delivery: An insight. Drug Targeting and Stimuli Sensitive Drug Delivery Systems, 117-154.
  • [18] Wood, J., Horton, A., Byrne, J., Pedroso, K., Bisnow, M., Auer, R. 1989. Flow Cytometry: Advanced Research Applications. (A. Yen, Ed.) Boca Raton, FL: CRC Press.
  • [19] Zhang, R., Qin, X., Kong, F., Chen, P., Pan, G. 2019. Improving cellular uptake of therapeutic entities through interaction with cell membrane components. Drug Deliv. 26(1):328-342.

In vitro Testing to Investigate Effects of Excipients in Drug Formulation

Yıl 2023, , 292 - 299, 15.08.2023
https://doi.org/10.22312/sdusbed.1328230

Öz

The formulation of drugs requires active pharmaceutical ingredients (API), which can be combined with some excipients, which are not considered pharmacologically active and could have different roles in a drug formulation. Glukofen, a generic name as a biguanide antidiabetic, is used for treating type 2 Diabetes Mellitus, mainly in overweight patients when dietary management and exercise do not help in adequate glycemic control. In Glukofen formulation, metformin-HCl as an API and some excipients such as povidone, magnesium stearate, hypromellose, and titanium dioxide are combined. The goal of this study is in vitro investigation of the effects of Glukofen and metformin-HCl on the human bronchial epithelial cell line (Beas-2b). To observe and compare their toxic effects and uptake into cells, cytotoxicity assay and flow cytometry experiments were carried out. The obtained results from this study showed that any toxic effects of both Glukofen and metformin-HCl on Beas-2b cells were not obtained. In addition, uptake of Glukofen into cells was observed more than metformin-HCl. It is evident that the incorporation of excipients to metformin-HCl results in a significant rise in cell proliferation and uptaking into cells.

Kaynakça

  • [1] Katny, M., Frankowski, M. 2016. Impurities in Drug Products and Active Pharmaceutical Ingredients. Critical Reviews in Analytical Chemistry, 47 (3), 187-193
  • [2] Jain, D., Basniwal, P. 2013. Forced degradation and impurity profiling: Recent trends in analytical perspectives. Journal of Pharmaceutical and Biomedical Analysis, 86, 11-35.
  • [3] Bardal, S., Waechter, J., Martin, D. 2011. Pharmacokinetics. In S. Bardal, J. Waechter, D. Martin, Applied Pharmacology (pp. 17-34). St. Louis, Missouri: Elsevier Saunders.
  • [4] Fortunak, J. M., de Souza, R. O., Kulkarni, A. A., King, C. L., Ellison, T., Miranda, L. S. 2014. Active pharmaceutical ingredients for antiretroviral treatment in low- and middle-income countries: a survey. Antiviral Therapy, 15-29.
  • [5] Fabiano, V., Mameli, C., Zuccotti, G. 2011. Pediatric Pharmacology: Remember the excipients. Pharmacological Research, 63 (5), 362-365.
  • [6] Hamman, J., Steenekamp, J. 2011. Excipients with specialized functions for effective drug delivery. Expert Opinion on Drug Delivery, 9 (2), 219-230.
  • [7] Çubuk, G., İnce, S. 2015. Oral Antidiyabetik İlaçlar. Kocatepe Veteriner Dergisi, 95-102.
  • [8] Li, C., Martini, L., Ford, J., & Roberts, M. 2005. The use of hypromellose in oral drug delivery. Journal of Pharmacy and Pharmacology, 57 (5), 533-546.
  • [9] Rowe, R. 1984. Materials used in the film coating of oral dosage forms. Critical Reports on Applied Chemistry, 6, 1-36.
  • [10] Adeyeye, C., Barabas, E. 1993. Excipient Profile: Povidone. In H. G. Brittain (Ed.), Analytical Profiles of Drug Substances and Excipients (Vol. 22, pp. 555-585). London: Academic Press.
  • [11] Butcher, A., Jones, T. 1972. Some physical characteristics of magnesium stearate. The Journal of Pharmacy and Pharmacology, 1P-9P.
  • [12] Lerk, C., Bolhuis, G., Smallenbroek, A., Zuurman, K. 1982. Interaction of tablet disintegrants and magnesium stearate during mixing. II. Effect on dissolution rate. Pharmaceutica acta Helvetiae, 282-286.
  • [13] Yen, FS., Wei, J.CC., Yang, YC. 2020. Respiratory outcomes of metformin use in patients with type 2 diabetes and chronic obstructive pulmonary disease. Scientific Reports, 10, 10298.
  • [14] Hinge, M A., Patel, KV. 2016. Development and Validation of Spectrophotometric Method for Metformin and Sitagliptin by Absorbance Ratio Method. J Pharm Sci Bioscientific Res. 6(5): 733-739.
  • [15] Holley, R. W. 1975. Control of growth of mammalian cells in cell culture. Nature, 487-490.
  • [16] Hansel, C., Barr, S., Schemann, A.V., Lauber, K., Hess, J., Unger, K., Zitzelsberger, H., Jendrossek, V., Klein, D. 2021. Metformin Protects against Radiation-Induced Acute Effects by Limiting Senescence of Bronchial-Epithelial Cells. International Journal of Science. 22, 7064.
  • [17] Pandey, P., Balekar, N. 2018. Target-specific Delivery: An insight. Drug Targeting and Stimuli Sensitive Drug Delivery Systems, 117-154.
  • [18] Wood, J., Horton, A., Byrne, J., Pedroso, K., Bisnow, M., Auer, R. 1989. Flow Cytometry: Advanced Research Applications. (A. Yen, Ed.) Boca Raton, FL: CRC Press.
  • [19] Zhang, R., Qin, X., Kong, F., Chen, P., Pan, G. 2019. Improving cellular uptake of therapeutic entities through interaction with cell membrane components. Drug Deliv. 26(1):328-342.
Toplam 19 adet kaynakça vardır.

Ayrıntılar

Birincil Dil İngilizce
Konular Eczacılık Biyokimyası
Bölüm Araştırma Makaleleri
Yazarlar

Hulya Yilmaz 0000-0003-4592-6432

Fatma Sertgöz 0000-0003-2963-5213

Ayse Cinkilic 0000-0002-1891-7349

Mustafa Culha 0000-0002-3844-5190

Yayımlanma Tarihi 15 Ağustos 2023
Gönderilme Tarihi 16 Temmuz 2023
Yayımlandığı Sayı Yıl 2023

Kaynak Göster

Vancouver Yilmaz H, Sertgöz F, Cinkilic A, Culha M. In vitro Testing to Investigate Effects of Excipients in Drug Formulation. Süleyman Demirel Üniversitesi Sağlık Bilimleri Dergisi. 2023;14(2):292-9.

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