Saritha AS, Santhosh RI (2015) Fast dissolving tablets using solid dispersion technique: an overview. Indo Am J Pharma Res 5(2):668–679
Hannan PA, Khan JA, Khan A, Safiullah S (2017) Oral dispersible systems: a new approach in drug delivery system. Ind J Pharm Sci 78:2–7
Pratik SD, Sushma V, Puja S (2017) Fast dissolving tablet using solid dispersion technique: a review. Int J Current Pharm Res 9(6):1–4
BhaskarR MO, Ravindra MG (2018) Review: solid dispersion techniques for enhancement of solubility of poorly soluble drug. Ind. J. Pharma Bio Res 6(2):43–52
Kumar B (2017) Solid Dispersion: A Review. Pharm Tutor 5(2):24–29
Sultana S, Saifuddin AHM (2016) Solid Dispersion: currently practiced in pharmaceutical field. Int. J. Adv Res Technol. 5(3):170–175
Mathew G, Lincy J, Pooran Mal S, Jyothilakshmi VN (2016) Research article on enhancing the bioavailability of poorly water soluble drug etoroxib using solid dispersion technique – solid dispersion a method to improve bioavailability of poorly water soluble drug. Int. J. Pharma Pharma. Res. 6(4):17–51
Allen LV, Levinson RS, Martono DD (1978). Dissolution Rates of Hydrocortisone and Prednisone utilizing sugar solid dispersion systems in tablet form. J. Pharm. Sci 67(7):979–981
Das SK, Roy S, Yuvaraj K, Khanam J (2011) Solid dispersion : an approach to enhance the bioavailability of poorly water soluble drugs. Int. J. Plastic Poly. Technol. 1(1):37–46
Leunner C, Dressman J (2000) Improving drug solubility for oral delivery using solid dispersions. Eur. J. Pharm. Biopharm 50(1):47–60
Ramesh V, Meenakshi S, Jyothirmayee N, Bullebbai M, Noorjahan SK, Rajeswari G, Nagesh Babu G, Madhavi D (2016) Enhancement of solubility, dissolution rate and bioavailability of BCS Class II Drugs. Int J Pharma Chem Res 2(2):80–95
Ghaderi R, Artursson P, Carlfors J (1996) Preparation of biodegradable microparticles using solution-enhanced dispersion by supercritical fluids (SEDS). Pharm. Research 16(5):676–681. https://doi.org/10.1023/A:1018868423309
Vasconcelos T, Sarmento B, Costa P (2007) Solid dispersions as strategy to improve oralbioavailability of poor water soluble drugs. Drug Discov. Today 12(23-24):1068–1075. https://doi.org/10.1016/j.drudis.2007.09.005
Pokharkar VB, Mandpe LP, Padamwar MN, Ambike AA, Mahadik KR, Paradkar A (2006) Development, characterization and stabilizationof amorphous form of a low Tg drug. Powder Technol 167(1):20–25. https://doi.org/10.1016/j.powtec.2006.05.012
Taylor LS, Zografi G (1997) Spectroscopic characterization of interactions between PVP and indomethacin in amorphous molecular dispersions. Pharm Res 14(12):1691–1698. https://doi.org/10.1023/A:1012167410376
Arias M J, Gines JM, Moyano JR, Rabasco AM. The application of solid dispersion technique withD-mannitol to the improvement in oral absorption of triamterene. J. Drug Target 2(1):45-51.
Sandip RP, Shashikant DE (2019) Solubility enhancement (Solid Dispersion) novel boon to increase bioavailability. J Drug Delivery Therapeutics 9(2):583–590
Mohd AF, Dilip KP, Kesharwani R (2018) A technique to enhance the bioavailability and solubility for poorly water soluble drugs by using solid dispersions. World J Pharm Pharm. Sci. 7(11):818–836
Younis AM (2017) Solid dispersion technology, a contemporary overview on a well-established technique. Uni. J. Pharm. Res. 2(3):2456–8058
Debjit BM, Chiranjib JJ, Vinod D, Margret C (2009) Fast dissolving tablet: a Review on revolution of novel drug delivery system and new market opportunities. Sch. Res. Library 1(2):262–276
Singh (2017) Solubility enhancement by solid dispersion. Ind. J. Pharm. Sci 79(5):674–687
Ramesh V, Meenakshi S (2016) Enhancement of solubility for poorly water soluble drugs by using solid dsipersion technology. Int. J. Pharm. Res Bio-Sci. 5(2):47–74
Allawadi D, Singh N, Singh S. And Arora S(2013). Solid dispersions: a review on drug delivery system and solubility enhancement. Int. J. Pharm. Sci. Res. 4(6):2094.
Singh J, Walia M. And Harikumar SL (2013). Solubility Enhancement by Solid Dispersion Method: A Review. J. Drug Delivery Therapeutics 3(5):148-155.
Midha, K., Rani, P. And Arora, G(2017). Solid dispersion: a recent update. Int J Pharm Pharmacol 1:104.
Vasconcelos T, Sarmento B. And Costa P (2007).Solid dispersions as strategy to improve oral bioavailability of poor water soluble drugs. Drug Discov. Today 12(23-24):1068-1075.
Katariya VR, Patil SB (2013) Recent breakthroughs in solid dispersion: a review. Int. J. Pharm. Res. Allied Sci. 2(4):1–15
Vo CLN, Park C, And Lee BJ (2013) Current trends and future perspectives of solid dispersions containing poorly water-soluble drugs. Eur. J. Pharm Biopharm. 85(3):799–813
Baghel S, Cathcart H. And Oreilly NJ (2016). Polymeric amorphous solid dispersions: a review of amorphization, crystallization, stabilization, solid-state characterization, and aqueous solubilization of biopharmaceutical classification system class II drugs. J. Pharm. Sci. 105(9):.2527-2544.
Bikiaris DN (2011) Solid dispersions, part i: recent evolutions and future opportunities in manufacturing methods for dissolution rate enhancement of poorly water-soluble drugs. Expert Opinion on Drug Delivery 8(11):1501–1519
Dixit ND, Niranjan SK (2014) A review: solid dispersion. World J. Pharm Pharm. Sci. 3(9):238–257
Kaur T, Gill B, Kumar S, Gupta GD (2011) Mouth dissolving tablets: a novel approach to drug delivery. Int. J. Curr. Pharm. Res. 1:1–7
Nagar P, Singh K, Chauhan I, Verma M, Yasir M, Khan A (2015) Orally disintegrating tablets: formulation, preparation techniques and evaluation. J. Appl. Pharm. Sci. 4:35–45
Kumaresan C (2015) Orally disintegrating tablet-mouth dissolving, sweet taste and target release profile. Pharmaceutical 6:25–36
Eun JK (2016) Preparation of solid dispersion of felodipine using a solvent wetting method. Eur. J. Pharm. Biopharm. 64:200–205
Shivalingam MR, Jyothibasu T, Kishore YV, Reddy A, Tejaswi B, Nagaanusha D (2011) Formulation and evaluation of solid dispersions of glipizide for dissolution rate enhancement. Int. J. Pharma. Res. Dev. 3(23):231–239
Prasad RS, Sarath KY, Manavalan R (2010) Preparation and characterization of itraconazole solid dispersions for improved oral bioavailability. Int. J. Chem. Tech. Res. 2(1):133–142
Kazi PA, Gholve SB, Kazi SN (2014) Review article solid dispersion: an evergreen method for solubility enhancement of poorly water soluble drugs. Int. J. Res. Pharm. Chem. 4:906–918
Sabitari B, Snehamayee M (2018) Recent research of solid dispersion: a new concept towards oral bioavailability. Asian J. Pharm. Clinical Res. 11(2):72–78
Gang Y, Zhao Y, Feng N, Zhang Y, Liu Y, Dang B (2015) Improved dissolution and bioavailability of silymarin delivered by a solid dispersion prepared using supercritical fluids. Asian J. Pharm. Sci. 10:194–204
Kaur P, Singh SK, Garg V, Gulati M, Vaidya Y (2015) Optimization of spray drying process for formulation of solid dispersion containing polypeptide-k powder through quality by design approach. Powder Technol. 284:1–11
Wei-Juan X, Xie HJ, Cao QR, Shi LL, Clao Y, Zhu XY (2016) Dissolution and oral bioavailability of valsartan solid dispersions prepared by a freeze-drying technique using hydrophilic polymer. J. Drug Delivery 23:41–48
Li J, Lee IW, Shin GH, Chen X, Park HJ (2015) Curcumin-eudragit® E PO solid dispersion: A simple and potent method to solve the problems of curcumin. Eur. J. Pharm. Biopharm. 94:322–332
Choi JS, Park JS (2015) Design of PVP/VA S-630 based tadalafil solid dispersion to enhance the dissolution rate. Eur. J. Pharm. Sci 97:269–276
Hacene YC, Singh A, Mooter GV (2016) Drug loaded and ethylcellulose coated mesoporous silica for controlled drug release prepared using a pilot scale fluid bed system. Int. J. Pharm. 506:138–147
Leung SS, Parumasivam T, Gao FG, Carrigy NB, Vehring R, Finlay WH (2016) Production of inhalation phage powders using spray freeze drying and spray drying techniques for treatment of respiratory infections. J. Pharm. Res 33:1486–1496
Rao P, Nagabhushanam MV, Prabhakar CH (2011) Enhancement of dissolution rate of poorly soluble drug mefenamic acid by solid dispersion. Res. J. Pharm. Bio. Chem. Sci. 2(3):1025–1035
Marano S, Barker SA, Raimi-Abraham BT, Missaghi S, Rajabi-Siahboomi A, Aliev AE (2017) Microfibrous solid dispersions of poorly water-soluble drugs produced via centrifugal spinning: Unexpected dissolution behavior on recrystallization. Mol. Pharm. 14:1666–1680
Bobe KR, Subrahmanya CR, Sarasija S, Gaikwad DT, Patil MD, Khade TS, Gavitre B, Kulkarni VS, Gaikwad UT (2011) Formulation and Evaluation of Solid Dispersion of Atorvastatin with Various Carriers. Int. J Comprehensive Pharma. 2(1):1–6
Roul LK, Manna NK, Parhi RN, Sahoo S, Suresh P (2012) Dissolution rate enhancement of alprazolam by solid dispersion. Ind. J. Pharm. Edu. and Res. 46(1):38–44
KPR. Chowdary KR, Kvnr. Aishwarya and Adilakshmi (2012). A factorial study on the enhancement of dissolution rate of aceclofenac by solid dispersion in starch phosphate and gelucire. Int. J Res Pharma. Chem.2(4):907-912.
Irin Dewan MD. Ayub H and Ashraful Islam SM (2012). Formulation and evaluation of solid dispersions of carvedilol, a poorly water soluble drug by using different polymers. Int. J Res Pharma. Chem. 2(3):585-593
Kumar P, Kumar S, Kumar A, Chander M (2010) Physicochemical characterization of solid dispersions of cefdinir with Pvp K-30 and Peg 4000. Int. J. Pharm. Sci Nanotechnol. 3(2):948–956
Deshmukh DB, Gaikwad PD, BankarVH PSP (2010) Dissolution enhancement of poorly water soluble diacereinby solid dispersion technique. J Pharm Sci Res 2(11):734–739
Abhisekh D, Amit Kumar N, Biswaranjanmohanty, and Satyabrata P (2011). Solubility and dissolution enhancement of etoricoxib by solid dispersion technique using sugar carriers. Int. Scholarly Res. Network Isrn Pharm. Article id 819765:1-8.
Chowdary KPR, Udaya Chandra D, Parimala V And Indira M (2012). A factorial study on formulation development of ibuprofen tablets employing starch 1500 and Pvp K 30. Int J Pharm Sci Res 3(1):189-193.
Subrata M, Ashok S, Kaushik P (2004) Dissolution behaviour of nalidix acid solid dispersions using water soluble dispersion carriers. Acta Poloniae Phrma. –Drug Res 61:21–30
Venkateskumar K, Arunkumar N, Verma P, Ranjan P, Siva P, Neema GAnd Punitha K (2011) Characterization of olanzapine-solid dispersions. Iran. J. Pharm. Res. 10(1):13–24
Vyas J, Vyas P, Patel J (2011) Formulation and evaluation of solid dispersions of rofecoxib for improvement of dissolution profile. Afr J. Pharm Pharmacology 5(5):577–581
Sukanya M, Sai Kishore V (2012) Design and development of solid dispersions of simvastatin for enhancing the solubility. Am J. Pharma. Tech. Res. 2(4):733–740
Dhat SP, Aphale SA, Sherje AP, Sakale JA, Vaidya AV, Vanshiv SD (2011) Solubility enhancement of satranidazole using solid dispersion technique. Int. J. Res. Pharm. Biomedical Sci. 2(3):1134–1135
Mohammed J, Dehghan M, Adil S (2010) Enhancementof dissolution and anti-inflammatory effect of meloxicam using solid dispersions. Int. J. Applied Pharm. 2(1):1–8
Sucheta B, Dyandevi M, Mithun VKP, Rajendra DP (2011) Solubility enhancement of antihypertensive agent by solid dispersion technique. International Journal of Pharmacy & Life Sciences. Int. J. Of Pharm Life Sci. 2(8):970–975
Gopal Venkatesh S, Averineni Ranjith K, Yogendra Nayak U, Karthik A, Om Prakash R, Kishore G, Sureshwar P, Nayababhirama U (2010) Enhanced dissolution and bioavailability of gliclazide using solid dispersion techniques. Int. J. Drug Delivery 2:49–57
Vinay P, Roopa SP, Kusum D, Saraija S (2012) In vitro-in vivo evaluation of fast-dissoliving tablets containing solid dispersion of pioglitazone hydrochloride. J. Adv. Pharm. Tech Res. 3(3):160–165
Renu K, Stuti G, Rajendra KRS, Dolly J, Sushma P (2011) Study of enhancement of dissolution rate of carbamazepine by solid dispersion. Int. J. Compr. Pharm. 5(9):1007–1014
Lalit J, Tapar KK (2011) Preparation and characterization of mesalamine solid dispersions by kneading method. Int. J. Pharm. Sci Res. 2(10):2623–2628
Nashwan YK, Alaaa A, Moafaq MG, Saad AH (2011) Solubility and dissolution improvement of ketoprofen by solid dispersion-polymer and surfactant using solvent evaporation method. Int. J. Pharm Pharm. Sci. 3(4):431–435
Yadav YB And Yadav AV (2009) Indomethacin solid dispersions by kneading method with lactose monohydrate and different polymers. J.Pharm. Res. 2(9):1489-1492.
Minhaz RA, Mofizur MD, Ahsan Q, Rahman H, Chowdhury R (2012) Enhancement of solubility and dissolution properties of clonazepam by solid dispersions. Int. J. Pharm. Life Sci. 3(3):1510–1515
Ramesh V, Rukesh KJ, Chowdary KPR (2015) Formulation of Telmisartan tablets employing solid dispersions in MCC PH102 and Poloxamer188 as per 22 factorial design. World J. Pharm. Res. 4(12):1397–1405
Ramesh V, Rukesh KJ, Chowdary KPR (2015) Formulation of Carvedilol tablets employing solid dispersions in MCC PH102 and Poloxamer188 as per 22 factorial design. World J. Pharm. Pharm. Sci. 5(2):753–762
Vivek D, Renu BY, Richa A, Atul KS (2017) Formulation and evaluation of orally dispersible tablets of Chlorpheniramine maleate by fusion method. Marmara Pharm. J 21:67–77. https://doi.org/10.12991/marupj.259883
Balasubramanian VM, Shaik AR, Kenneti NM, Muuva A, Nadendla RR (2017) Formulation and evaluation of mouth dissolving tablets of telmisartan by solid dispersion technique. Asian J. of Res. Chem Pharm. Sci. 5(1):38–49
Singh G, Kaur L, Gupta GD (2017) Enhancement of the solubility of poorly soluble drugs through solid dispersion: A comprehensive review. Ind. J. Pharm. Sci. 79(5):674–687
Allen LVJ, Yanchick VA, Maness DD (1997) Dissolution rates of corticosteriods utilizing sugar glass dispersions. J. Pharm. Sci 66(4):494–496
Ratnaparkhil MP, Mohanta GP, Upadhyay L (2009) Review on: Fast Dissolving Tablet. J. Pharm. Res. 2(1):5–12
Amidon GL, Lennernas H, Shah VP, Crison JR (1995) Theoretical basis for a biopharmaceutic drug classification the correlation of in vitro drug product dissolution and in vivo bioavailability. Pharm. Res. 3(12):413–420
Shaik AR (2015) Pharmaceutical drug classification: the correlation of in vitro drug product dissolution and in vivo bioavailability. Pharm Res. 12(3):413–420
Shyamala B, Narmada GY (2002) Rapid dissolving tablets: a novel dosage form. The Ind. Pharmacist. 13(8):09–12
Anne MJ, Catherine B, Cynthia K (2003) Evaluation of solid dispersion particles prepared with SEDS. Int. J. of Pharm. 250:385–401