Amplification of Aqueous Solubility of Progesterone Using Melt- Granulation Technique
Bhosale DS*, Kalshetti MS
DSTS Mandal’s College of Pharmacy, Solapur, Maharashtra, India.
Received: 12th September, 2023; Revised: 30th January, 2024; Accepted: 15th February, 2024; Available Online: 25th March, 2024
ABSTRACT
The objective of the present research was to enhance the rate of dissolution of progesterone by boosting the hormone’s solubility in water. This research determines whether or not employing melt granulation techniques with various polymers may improve the degree to which progesterone is soluble. When looking into the interactions between drug carriers and other substances, researchers turned to techniques such as X-ray diffraction (XRD), differential scanning calorimetry (DSC), and Fourier transform infrared (FTIR). PEG 6000 (1:1.5) demonstrated the highest solubility, followed by PEG 6000 (1:1) > Gelucire 50/13 (1:1.5) > Gelucire 50/13 (1:1). Increasing the solubility of the weakly soluble progesterone was demonstrated by these findings. Melt granulation on polymers boosted progesterone’s dissolution rate, which in turn can raise oral bioavailability.
Keywords: Progesterone, Bioavailability, Gelucire, PEG 6000, solubility.
International Journal of Drug Delivery Technology (2024); DOI: 10.25258/ijddt.14.1.05
How to cite this article: Bhosale DS, Kalshetti MS. Amplification of Aqueous Solubility of Progesterone Using Melt- Granulation Technique. International Journal of Drug Delivery Technology. 2024;14(1):26-32.
REFERENCES
- Vasconcelos T, Sarmento B, Costa Solid dispersions as strategy to improve oral bioavailability of poor water-soluble drugs. Drug discovery today. 2007 Dec 1;12(23-24):1068-75. https:// doi.org/10.1016/j.drudis.2007.09.005.
- Butreddy A, Sarabu S, Almutairi M, Ajjarapu S, Kolimi P, Bandari S, Repka MA. Hot-melt extruded hydroxypropyl methylcellulose acetate succinate based amorphous solid dispersions: Impact of polymeric combinations on supersaturation kinetics and dissolution performance. International Journal of 2022 Mar 5;615:121471. https://doi.org/10.1016/j. ijpharm.2022.121471
- Argade PS, Magar DD, Saudagar Solid dispersion: solubility enhancement technique for poorly water-soluble drugs. Journal of Advanced Pharmacy Education & Research. 2013 Oct;3(4):427- 439
- Madan JR, Kamate VJ, Dua K, Awasthi R. Improving the solubility of nevirapine using a hydrotropy and mixed hydrotropy based solid dispersion approach. Polymers in Medicine. 2017;47(2):83-90. https://doi.org/10.17219/pim/77093.
- Mamatha P, Bhikshapathi DVRN. Preparation and In-vitro Evaluation of Pemigatinib Nanosponges Tablets by Box- Behnken Design. International Journal of Pharmaceutical Quality 2023;14(3):791-800. https://doi.org/10.25258/ ijpqa.14.3.56.
- Kshirsagar S, Choudhari M, Sathyan R, Dhore S. Solubility enhancement by various techniques based on pharmaceutical and medicinal chemistry approach: an overview. Asian Journal of Pharmacy and Technology. 2019;9(2):141-6. https://doi. org/10.5958/2231-5713.2019.00024.2
- Sahoo CK, Reddy GS, Vojjala A, Reddy BV. Bioavailability enhancement for poorly soluble drugs: A review. Innoriginal: International Journal of Sciences. 2018 Jun 6:1-6.
- Dhillon B, Goyal NK, Malviya R, Sharma PK. Poorly water- soluble drugs: Change in solubility for improved dissolution characteristics a review. Global Journal of Pharmacology. 2014;8(1):26-35. https://doi.org/10.5829/idosi.gjp.2014.8.1.81201
- Moinuddin, Neekhra S, Ahmad S, Swarnkar SK, Gupta D, Khunteta A, Jain P, Jain S. Evaluation of Oral Bioavailability and In-vivo Anti-leukemic Potential of Dasatinib Loaded Solid Lipid Nanoparticles. International Journal of Pharmaceutical Quality 2023;14(3):587-591. https://doi.org/10.25258/ijpqa.14.3.21.
- Lopez RA, Goodman AB, Rhodes M, Blomberg JA, Heller J. The anticancer activity of the transcription inhibitor terameprocol (meso-tetra-O-methyl nordihydroguaiaretic acid) formulated for systemic administration. Anti-cancer drugs. 2007 Sep 1;18(8):933-9. https://doi.org/10.1097/CAD.0b013e32813148e0.
- Chen X, Partheniadis I, Nikolakakis I, Al-Obaidi H. Solubility improvement of progesterone from solid dispersions prepared by solvent evaporation and co-milling. Polymers. 2020 Apr 7;12(4):854. https://doi.org/10.3390/polym12040854
- Kannao SU, Bakade BV. Solid Dispersion–A Technique for Solubility Enhancement of Weakly Water-Soluble Drug–A Review. Indo American Journal of Pharm Research. 2014;4(6).
- Narala S, Komanduri N, Nyavanandi D, Youssef AA, Mandati P, Alzahrani A, Kolimi P, Narala N, Repka MA. Hard gelatin capsules containing hot melt extruded solid crystal suspension of carbamazepine for improving dissolution: Preparation and in vitro evaluation. Journal of Drug Delivery Science and Technology. 2023 Apr 1;82:104384. https://doi.org/10.1016/j. 2023.104384
- Rodge PJ, Shirolkar Solubility Enhancement of Itraconazole by Centrifugal Melt Spinning Technique. International Journal of Drug Delivery Technology. 2023;13(3):812-817. https://doi. org/10.25258/ijddt.13.3.06
- Rincón-López J, Almanza-Arjona YC, Riascos AP, Rojas- Aguirre Y. Technological evolution of cyclodextrins in the pharmaceutical field. Journal of Drug Delivery Science and Technology. 2021 Feb 1; 61:102156. https://doi.org/10.1016/j. 2020.102156