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References
- Alhasani, K.F, Kazi M, Ibrahim, M.A, Shahba, A. A, Alanazi, F.K. (2019) ‘Self-nanoemulsifying ramipril tablets: A novel delivery system for the enhancement of drug dissolution and stability’, International Journal of Nanomedicine, 14, pp. 5435–5448. Available at: https://doi.org/10.2147/IJN.S203311.
- BPOM RI. (2011) ‘Obat Wajib Uji Ekivalensi’, Badan Pengawas Obat dan Makanan Republik Indonesia.
- Budiman, M.F. (2019) ‘Preparasi dan Karakterisasi Tablet Liquisolid Ramipril’, Tesis, Sekolah Farmasi Institut Teknologi Bandung.
- Dhall, M., Phaugat, P. and Nishal, S. (2019) ‘Studies on refined liquisolid system for simultaneous improvement of content uniformity and dissolution profile of glimepiride’, International Journal of Applied Pharmaceutics, 11(4), pp. 396–405. Available at: https://doi.org/10.22159/ijap.2019v11i4.33025.
- FDA. 2011, ‘Tablet Ramipril’, Food and Drug Administration, https://www.accesdata.fda.gov/drugsatfda_docs/label/2011/022021s007lbl.pdf, Diakses pada 2 Juli 2021
- Kemenkes RI. (2020) ‘Farmakope Indonesia Edisi VI’, Kementerian Kesehatan Republik Indonesia.
- Hay, A.M.A.El. and Adawy, Sh.A.El. (2017) ‘Enhancement of Dissolution Rate of Ramipril Tablets by Solid Dispersion Technique’, IOSR Journal of Pharmacy and Biological Sciences, 12(03), pp. 55–62. Available at: https://doi.org/10.9790/3008-1203015562.
- Jayapal, N. and Vamshi V. Y. (2021) ‘Formulation and In Vivo Evaluation of Self-Nanoemulsifying Drug Delivery System of Ramipril in Wistar Rats’, Asian Journal of Pharmaceutical and Clinical Research, 14(7), pp. 126-136. Available at: https://doi.org/10.22159/ajpcr.2021v14i7.42003.
- Kawabata, Y., Wada, K., Nakatani, M., Yamada, S., Onoue, S. (2011) ‘Formulation design for poorly water-soluble drugs based on biopharmaceutics classification system: Basic approaches and practical applications’, International Journal of Pharmaceutics. Elsevier B.V., pp. 1–10. Available at: https://doi.org/10.1016/j.ijpharm.2011.08.032.
- Kumar, I., Verma, S. and Chaudhary, A. (2020) ‘Formulation of Ramipril Tablets Containing Solid Dispersion Employing Selective Polymers to Enhance Dissolution Rate’, Journal of Drug Delivery and Therapeutics, 10(3-s), pp. 142–149. Available at: https://doi.org/10.22270/jddt.v10i3-s.4109.
- Nirmala, M.J., Allanki, S., Mukherjee, A., Chandrasekaran, N. (2013) ‘Enhancing The Solubility of Ramipril Using a New Essential Oil Based Microemulsion System’, International Journal of Pharmacy and Pharmaceutical Science. 5(4), pp.322-323
- Santosh Kumar, R. and Sai, J.D. (2019) ‘Liquisolid Compacts: A Review’, Journal of Drug Delivery and Therapeutics, 9, p. 4. Available at: https://doi.org/10.22270/jddt.v9i4-A.3706.
- Shafiq, S., Shakeel, F., Talegaonkar, S., Ahmad, F.J., Khar, R.K., Ali, M. (2007) ‘Development and bioavailability assessment of ramipril nanoemulsion formulation’, European Journal of Pharmaceutics and Biopharmaceutics, 66(2), pp. 227–243. Available at: https://doi.org/10.1016/j.ejpb.2006.10.014.
- Shahba, A.A.W., Sherif, A., Ellzayat, E.M., Kazi, M. (2022) ‘Combined Ramipril and Black Seed Oil Dosage Forms Using Bioactive Self-Nanoemulsifying Drug Delivery Systems (BIO-SNEDDSs)’, Pharmaceuticals, 15(9). Available at: https://doi.org/10.3390/ph15091120.
- Siju, V.V., and Soniwala, M. (2017) ‘Liquisolid Compact: A New Technology for Optimization of Paliperidone Tablets by Central Composite Design’, International Journal of Pharmaceutical Sciences Review and Research, 45(1), pp.11-17
- Spireas, S. (2002) ‘Liquidsolid System and Methods of Preparation Same’, Pharmaceutical Research, 9, pp. 1-6.
- Suryawanshi, V. K., Gidwani, B., Verma, A., Dubey, N., Kaur, C. D. (2019) ‘Formulation and Evaluation of Ramipril Liquisolid Compact Using Novel Carrier’, International Journal of Pharmaceutical Sciences and Research, 10(2), pp. 917–925. Available at: https://doi.org/10.13040/IJPSR.0975-8232.10(2).917-25.
- Venkatesh, N., Thapa, A., Goti, S., Awari, V.P., Kalro, K.D. (2016) ‘Dissolution enhancement of ramipril using water soluble carrier by solid dispersion technology’, Journal of Pharmacy Research, 5(7), pp. 3561–3566. Available at: http://jprsolutions.info.
- VranÃková, B., Gajdziok, J. and Vetchý, D. (2015) ‘Modern evaluation of liquisolid systems with varying amounts of liquid phase prepared using two different methods’, BioMed Research International, Available at: https://doi.org/10.1155/2015/608435.
- Wang, D. et al. (2017) ‘Liquisolid technique and its applications in pharmaceutics’, Asian Journal of Pharmaceutical Sciences, pp. 115–123. Available at: https://doi.org/10.1016/j.ajps.2016.09.007.
References
Alhasani, K.F, Kazi M, Ibrahim, M.A, Shahba, A. A, Alanazi, F.K. (2019) ‘Self-nanoemulsifying ramipril tablets: A novel delivery system for the enhancement of drug dissolution and stability’, International Journal of Nanomedicine, 14, pp. 5435–5448. Available at: https://doi.org/10.2147/IJN.S203311.
BPOM RI. (2011) ‘Obat Wajib Uji Ekivalensi’, Badan Pengawas Obat dan Makanan Republik Indonesia.
Budiman, M.F. (2019) ‘Preparasi dan Karakterisasi Tablet Liquisolid Ramipril’, Tesis, Sekolah Farmasi Institut Teknologi Bandung.
Dhall, M., Phaugat, P. and Nishal, S. (2019) ‘Studies on refined liquisolid system for simultaneous improvement of content uniformity and dissolution profile of glimepiride’, International Journal of Applied Pharmaceutics, 11(4), pp. 396–405. Available at: https://doi.org/10.22159/ijap.2019v11i4.33025.
FDA. 2011, ‘Tablet Ramipril’, Food and Drug Administration, https://www.accesdata.fda.gov/drugsatfda_docs/label/2011/022021s007lbl.pdf, Diakses pada 2 Juli 2021
Kemenkes RI. (2020) ‘Farmakope Indonesia Edisi VI’, Kementerian Kesehatan Republik Indonesia.
Hay, A.M.A.El. and Adawy, Sh.A.El. (2017) ‘Enhancement of Dissolution Rate of Ramipril Tablets by Solid Dispersion Technique’, IOSR Journal of Pharmacy and Biological Sciences, 12(03), pp. 55–62. Available at: https://doi.org/10.9790/3008-1203015562.
Jayapal, N. and Vamshi V. Y. (2021) ‘Formulation and In Vivo Evaluation of Self-Nanoemulsifying Drug Delivery System of Ramipril in Wistar Rats’, Asian Journal of Pharmaceutical and Clinical Research, 14(7), pp. 126-136. Available at: https://doi.org/10.22159/ajpcr.2021v14i7.42003.
Kawabata, Y., Wada, K., Nakatani, M., Yamada, S., Onoue, S. (2011) ‘Formulation design for poorly water-soluble drugs based on biopharmaceutics classification system: Basic approaches and practical applications’, International Journal of Pharmaceutics. Elsevier B.V., pp. 1–10. Available at: https://doi.org/10.1016/j.ijpharm.2011.08.032.
Kumar, I., Verma, S. and Chaudhary, A. (2020) ‘Formulation of Ramipril Tablets Containing Solid Dispersion Employing Selective Polymers to Enhance Dissolution Rate’, Journal of Drug Delivery and Therapeutics, 10(3-s), pp. 142–149. Available at: https://doi.org/10.22270/jddt.v10i3-s.4109.
Nirmala, M.J., Allanki, S., Mukherjee, A., Chandrasekaran, N. (2013) ‘Enhancing The Solubility of Ramipril Using a New Essential Oil Based Microemulsion System’, International Journal of Pharmacy and Pharmaceutical Science. 5(4), pp.322-323
Santosh Kumar, R. and Sai, J.D. (2019) ‘Liquisolid Compacts: A Review’, Journal of Drug Delivery and Therapeutics, 9, p. 4. Available at: https://doi.org/10.22270/jddt.v9i4-A.3706.
Shafiq, S., Shakeel, F., Talegaonkar, S., Ahmad, F.J., Khar, R.K., Ali, M. (2007) ‘Development and bioavailability assessment of ramipril nanoemulsion formulation’, European Journal of Pharmaceutics and Biopharmaceutics, 66(2), pp. 227–243. Available at: https://doi.org/10.1016/j.ejpb.2006.10.014.
Shahba, A.A.W., Sherif, A., Ellzayat, E.M., Kazi, M. (2022) ‘Combined Ramipril and Black Seed Oil Dosage Forms Using Bioactive Self-Nanoemulsifying Drug Delivery Systems (BIO-SNEDDSs)’, Pharmaceuticals, 15(9). Available at: https://doi.org/10.3390/ph15091120.
Siju, V.V., and Soniwala, M. (2017) ‘Liquisolid Compact: A New Technology for Optimization of Paliperidone Tablets by Central Composite Design’, International Journal of Pharmaceutical Sciences Review and Research, 45(1), pp.11-17
Spireas, S. (2002) ‘Liquidsolid System and Methods of Preparation Same’, Pharmaceutical Research, 9, pp. 1-6.
Suryawanshi, V. K., Gidwani, B., Verma, A., Dubey, N., Kaur, C. D. (2019) ‘Formulation and Evaluation of Ramipril Liquisolid Compact Using Novel Carrier’, International Journal of Pharmaceutical Sciences and Research, 10(2), pp. 917–925. Available at: https://doi.org/10.13040/IJPSR.0975-8232.10(2).917-25.
Venkatesh, N., Thapa, A., Goti, S., Awari, V.P., Kalro, K.D. (2016) ‘Dissolution enhancement of ramipril using water soluble carrier by solid dispersion technology’, Journal of Pharmacy Research, 5(7), pp. 3561–3566. Available at: http://jprsolutions.info.
VranÃková, B., Gajdziok, J. and Vetchý, D. (2015) ‘Modern evaluation of liquisolid systems with varying amounts of liquid phase prepared using two different methods’, BioMed Research International, Available at: https://doi.org/10.1155/2015/608435.
Wang, D. et al. (2017) ‘Liquisolid technique and its applications in pharmaceutics’, Asian Journal of Pharmaceutical Sciences, pp. 115–123. Available at: https://doi.org/10.1016/j.ajps.2016.09.007.