Skip to main content
Top
Published in: Journal of Polymer Research 7/2019

01-07-2019 | ORIGINAL PAPER

Preparation and in vitro characterization of polyvinylpyrrolidone-poloxamer polymeric synergy for oral drug delivery

Authors: Saman Ali, Abid Mehmood Yousaf, Syed Atif Raza, Yasser Shahzad, Ikram Ullah Khan, Tariq Mahmood, Talib Hussain, Mobina Manzoor, Humayun Riaz, Muhammad Jamshaid

Published in: Journal of Polymer Research | Issue 7/2019

Log in

Activate our intelligent search to find suitable subject content or patents.

search-config
loading …

Abstract

The prospect of carrying out this study was to prepare and characterize an optimized polyvinylpyrrolidone (PVP)-poloxamer (PLX) hydrophilic polymeric blend for improved solubility of poorly water-soluble drugs. Levodropropizine (LDP) was used as a model drug in this research. Several LDP-loaded PVP-PLX formulations were fabricated via the solvent evaporation method, and tested for solubility and dissolution of LDP in water. Other physicochemical characterization was accomplished using X-ray diffraction (XRD), differential scanning calorimetry (DSC), scanning electron microscopy (SEM) and Fourier transform infrared spectroscopy (FTIR). Amongst all the formulations tested, the one composed of LDP, PVP and PLX at the ratio of 25/37.5/37.5 (w/w/w, %) gave the highest solubility (~ 470.96 ± 23.84 mg/ml) and dissolution (~ 95% in 15 min) of LDP in the aqueous media. Furthermore, LDP existed in the amorphous state in this formulation with no strong chemical interactions with the components of polymeric blend. The morphological investigations revealed that the particles of this formulation had irregular shapes and surfaces. Thus, the abovementioned optimized hydrophilic polymeric blend, composite or synergist might be a suitable oral delivery system for numerous other poorly water-soluble drugs as well.

Dont have a licence yet? Then find out more about our products and how to get one now:

Springer Professional "Wirtschaft+Technik"

Online-Abonnement

Mit Springer Professional "Wirtschaft+Technik" erhalten Sie Zugriff auf:

  • über 102.000 Bücher
  • über 537 Zeitschriften

aus folgenden Fachgebieten:

  • Automobil + Motoren
  • Bauwesen + Immobilien
  • Business IT + Informatik
  • Elektrotechnik + Elektronik
  • Energie + Nachhaltigkeit
  • Finance + Banking
  • Management + Führung
  • Marketing + Vertrieb
  • Maschinenbau + Werkstoffe
  • Versicherung + Risiko

Jetzt Wissensvorsprung sichern!

Springer Professional "Technik"

Online-Abonnement

Mit Springer Professional "Technik" erhalten Sie Zugriff auf:

  • über 67.000 Bücher
  • über 390 Zeitschriften

aus folgenden Fachgebieten:

  • Automobil + Motoren
  • Bauwesen + Immobilien
  • Business IT + Informatik
  • Elektrotechnik + Elektronik
  • Energie + Nachhaltigkeit
  • Maschinenbau + Werkstoffe




 

Jetzt Wissensvorsprung sichern!

Literature
1.
go back to reference Yousaf AM, Malik UR, Shahzad Y, Mahmood T, Hussain T (2018) Silymarin-laden PVP-PEG polymeric composite for enhanced aqueous solubility and dissolution rate: preparation and in vitro characterization. J Pharm Anal 9(1):34–39CrossRef Yousaf AM, Malik UR, Shahzad Y, Mahmood T, Hussain T (2018) Silymarin-laden PVP-PEG polymeric composite for enhanced aqueous solubility and dissolution rate: preparation and in vitro characterization. J Pharm Anal 9(1):34–39CrossRef
2.
go back to reference Li M, Rouaud O, Poncelet D (2008) Microencapsulation by solvent evaporation: state of the art for process engineering approaches. Int J Pharm 363(1–2):26–39CrossRef Li M, Rouaud O, Poncelet D (2008) Microencapsulation by solvent evaporation: state of the art for process engineering approaches. Int J Pharm 363(1–2):26–39CrossRef
3.
go back to reference Brewster ME, Loftsson T (2007) Cyclodextrins as pharmaceutical solubilizers. Adv Drug Deliv Rev 59(7):645–666CrossRef Brewster ME, Loftsson T (2007) Cyclodextrins as pharmaceutical solubilizers. Adv Drug Deliv Rev 59(7):645–666CrossRef
4.
go back to reference Yousaf AM, Kim DW, Oh Y-K, Yong CS, Kim JO, Choi H-G (2015) Enhanced oral bioavailability of fenofibrate using polymeric nanoparticulated systems: physicochemical characterization and in vivo investigation. Int J Nanomedicine 10:1819–1830PubMedPubMedCentral Yousaf AM, Kim DW, Oh Y-K, Yong CS, Kim JO, Choi H-G (2015) Enhanced oral bioavailability of fenofibrate using polymeric nanoparticulated systems: physicochemical characterization and in vivo investigation. Int J Nanomedicine 10:1819–1830PubMedPubMedCentral
5.
go back to reference Lawrence MJ, Rees GD (2012) Microemulsion-based media as novel drug delivery systems. Adv Drug Deliv Rev 64:175–193CrossRef Lawrence MJ, Rees GD (2012) Microemulsion-based media as novel drug delivery systems. Adv Drug Deliv Rev 64:175–193CrossRef
6.
go back to reference Gursoy RN, Benita S (2004) Self-emulsifying drug delivery systems (SEDDS) for improved oral delivery of lipophilic drugs. Biomed Pharmacother 58(3):173–182CrossRef Gursoy RN, Benita S (2004) Self-emulsifying drug delivery systems (SEDDS) for improved oral delivery of lipophilic drugs. Biomed Pharmacother 58(3):173–182CrossRef
7.
go back to reference Yang T, Cui F-D, Choi M-K, Cho J-W, Chung S-J, Shim C-K, Kim D-D (2007) Enhanced solubility and stability of PEGylated liposomal paclitaxel: in vitro and in vivo evaluation. Int J Pharm 338(1–2):317–326CrossRef Yang T, Cui F-D, Choi M-K, Cho J-W, Chung S-J, Shim C-K, Kim D-D (2007) Enhanced solubility and stability of PEGylated liposomal paclitaxel: in vitro and in vivo evaluation. Int J Pharm 338(1–2):317–326CrossRef
8.
go back to reference Jadon PS, Gajbhiye V, Jadon RS, Gajbhiye KR, Ganesh N (2009) Enhanced oral bioavailability of griseofulvin via niosomes. AAPS PharmSciTech 10(4):1186–1192CrossRef Jadon PS, Gajbhiye V, Jadon RS, Gajbhiye KR, Ganesh N (2009) Enhanced oral bioavailability of griseofulvin via niosomes. AAPS PharmSciTech 10(4):1186–1192CrossRef
9.
go back to reference Gupta U, Agashe HB, Asthana A, Jain N (2006) Dendrimers: novel polymeric nanoarchitectures for solubility enhancement. Biomacromolecules 7(3):649–658CrossRef Gupta U, Agashe HB, Asthana A, Jain N (2006) Dendrimers: novel polymeric nanoarchitectures for solubility enhancement. Biomacromolecules 7(3):649–658CrossRef
10.
go back to reference Vasconcelos T, Sarmento B, Costa P (2007) Solid dispersions as strategy to improve oral bioavailability of poor water soluble drugs. Drug Discov Today 12(23–24):1068–1075CrossRef Vasconcelos T, Sarmento B, Costa P (2007) Solid dispersions as strategy to improve oral bioavailability of poor water soluble drugs. Drug Discov Today 12(23–24):1068–1075CrossRef
11.
go back to reference Obaidat RM, AlTaani B, Ailabouni A (2017) Effect of different polymeric dispersions on in-vitro dissolution rate and stability of celecoxib class II drug. J Polym Res 24(4):58CrossRef Obaidat RM, AlTaani B, Ailabouni A (2017) Effect of different polymeric dispersions on in-vitro dissolution rate and stability of celecoxib class II drug. J Polym Res 24(4):58CrossRef
12.
go back to reference Yousaf AM, Ramzan M, Shahzad Y, Mahmood T, Jamshaid M (2019) Fabrication and in vitro characterization of fenofibric acid-loaded hyaluronic acid–polyethylene glycol polymeric composites with enhanced drug solubility and dissolution rate. Int J Polym Mater Polym Biomater 68(9):510–515CrossRef Yousaf AM, Ramzan M, Shahzad Y, Mahmood T, Jamshaid M (2019) Fabrication and in vitro characterization of fenofibric acid-loaded hyaluronic acid–polyethylene glycol polymeric composites with enhanced drug solubility and dissolution rate. Int J Polym Mater Polym Biomater 68(9):510–515CrossRef
13.
go back to reference Modi A, Tayade P (2006) Enhancement of dissolution profile by solid dispersion (kneading) technique. AAPS PharmSciTech 7(3):E87–E92CrossRef Modi A, Tayade P (2006) Enhancement of dissolution profile by solid dispersion (kneading) technique. AAPS PharmSciTech 7(3):E87–E92CrossRef
14.
go back to reference Hasegawa S, Hamaura T, Furuyama N, Kusai A, Yonemochi E, Terada K (2005) Effects of water content in physical mixture and heating temperature on crystallinity of troglitazone-PVP K30 solid dispersions prepared by closed melting method. Int J Pharm 302(1–2):103–112CrossRef Hasegawa S, Hamaura T, Furuyama N, Kusai A, Yonemochi E, Terada K (2005) Effects of water content in physical mixture and heating temperature on crystallinity of troglitazone-PVP K30 solid dispersions prepared by closed melting method. Int J Pharm 302(1–2):103–112CrossRef
15.
go back to reference Leuner C, Dressman J (2000) Improving drug solubility for oral delivery using solid dispersions. Eur J Pharm Biopharm 50(1):47–60CrossRef Leuner C, Dressman J (2000) Improving drug solubility for oral delivery using solid dispersions. Eur J Pharm Biopharm 50(1):47–60CrossRef
16.
go back to reference Pathak D, Dahiya S, Pathak K (2008) Solid dispersion of meloxicam: Factorially designed dosage form for geriatric population. Acta Pharma 58(1):99–110CrossRef Pathak D, Dahiya S, Pathak K (2008) Solid dispersion of meloxicam: Factorially designed dosage form for geriatric population. Acta Pharma 58(1):99–110CrossRef
17.
go back to reference Kim E-J, Chun M-K, Jang J-S, Lee I-H, Lee K-R, Choi H-K (2006) Preparation of a solid dispersion of felodipine using a solvent wetting method. Eur J Pharm Biopharm 64(2):200–205CrossRef Kim E-J, Chun M-K, Jang J-S, Lee I-H, Lee K-R, Choi H-K (2006) Preparation of a solid dispersion of felodipine using a solvent wetting method. Eur J Pharm Biopharm 64(2):200–205CrossRef
18.
go back to reference Hugo M, Kunath K, Dressman J (2013) Selection of excipient, solvent and packaging to optimize the performance of spray-dried formulations: case example fenofibrate. Drug Dev Ind Pharm 39(2):402–412CrossRef Hugo M, Kunath K, Dressman J (2013) Selection of excipient, solvent and packaging to optimize the performance of spray-dried formulations: case example fenofibrate. Drug Dev Ind Pharm 39(2):402–412CrossRef
19.
go back to reference Taylor LS, Zografi G (1997) Spectroscopic characterization of interactions between PVP and indomethacin in amorphous molecular dispersions. Pharm Res 14(12):1691–1698CrossRef Taylor LS, Zografi G (1997) Spectroscopic characterization of interactions between PVP and indomethacin in amorphous molecular dispersions. Pharm Res 14(12):1691–1698CrossRef
20.
go back to reference Doherty C, York P (1989) Accelerated stability of an X-ray amorphous frusemide-polyvinylpyrrolidone solid dispersion. Drug Dev Ind Pharm 15(12):1969–1987CrossRef Doherty C, York P (1989) Accelerated stability of an X-ray amorphous frusemide-polyvinylpyrrolidone solid dispersion. Drug Dev Ind Pharm 15(12):1969–1987CrossRef
21.
go back to reference Konno H, Handa T, Alonzo DE, Taylor LS (2008) Effect of polymer type on the dissolution profile of amorphous solid dispersions containing felodipine. Eur J Pharm Biopharm 70(2):493–499CrossRef Konno H, Handa T, Alonzo DE, Taylor LS (2008) Effect of polymer type on the dissolution profile of amorphous solid dispersions containing felodipine. Eur J Pharm Biopharm 70(2):493–499CrossRef
22.
go back to reference Gupta P, Kakumanu VK, Bansal AK (2004) Stability and solubility of celecoxib-PVP amorphous dispersions: a molecular perspective. Pharm Res 21(10):1762–1769CrossRef Gupta P, Kakumanu VK, Bansal AK (2004) Stability and solubility of celecoxib-PVP amorphous dispersions: a molecular perspective. Pharm Res 21(10):1762–1769CrossRef
23.
go back to reference Tanno F, Nishiyama Y, Kokubo H, Obara S (2004) Evaluation of hypromellose acetate succinate (HPMCAS) as a carrier in solid dispersions. Drug Dev Ind Pharm 30(1):9–17CrossRef Tanno F, Nishiyama Y, Kokubo H, Obara S (2004) Evaluation of hypromellose acetate succinate (HPMCAS) as a carrier in solid dispersions. Drug Dev Ind Pharm 30(1):9–17CrossRef
24.
go back to reference Yousaf AM, Kim DW, Kim DS, Kim JO, Youn YS, Cho KH, Yong CS, Choi H-G (2016) Influence of polyvinylpyrrolidone quantity on the solubility, crystallinity and oral bioavailability of fenofibrate in solvent-evaporated microspheres. J Microencapsul 33(4):365–371CrossRef Yousaf AM, Kim DW, Kim DS, Kim JO, Youn YS, Cho KH, Yong CS, Choi H-G (2016) Influence of polyvinylpyrrolidone quantity on the solubility, crystallinity and oral bioavailability of fenofibrate in solvent-evaporated microspheres. J Microencapsul 33(4):365–371CrossRef
25.
go back to reference Kubo H, Mizobe M (1997) Improvement of dissolution rate and Oral bioavailability of a sparingly water-soluble drug, (±)-5-[[2-(2-Naphthalenylmethyl)-5-benzoxazolyl]-methyl]-2, 4,-thiazolidinedione, in co-ground mixture with D-mannitol. Biol Pharm Bull 20(4):460–463CrossRef Kubo H, Mizobe M (1997) Improvement of dissolution rate and Oral bioavailability of a sparingly water-soluble drug, (±)-5-[[2-(2-Naphthalenylmethyl)-5-benzoxazolyl]-methyl]-2, 4,-thiazolidinedione, in co-ground mixture with D-mannitol. Biol Pharm Bull 20(4):460–463CrossRef
26.
go back to reference Chow AH, Hsia CK, Gordon JD, Young JW, Vargha-Butler EI (1995) Assessment of wettability and its relationship to the intrinsic dissolution rate of doped phenytoin crystals. Int J Pharm 126(1–2):21–28CrossRef Chow AH, Hsia CK, Gordon JD, Young JW, Vargha-Butler EI (1995) Assessment of wettability and its relationship to the intrinsic dissolution rate of doped phenytoin crystals. Int J Pharm 126(1–2):21–28CrossRef
27.
go back to reference El Sayed AM, Mohamad ADM (2018) Synthesis, structural, thermal, optical and dielectric properties of chitosan biopolymer; influence of PVP and α-Fe2O3 Nanorods. J Polym Res 25(8):175CrossRef El Sayed AM, Mohamad ADM (2018) Synthesis, structural, thermal, optical and dielectric properties of chitosan biopolymer; influence of PVP and α-Fe2O3 Nanorods. J Polym Res 25(8):175CrossRef
28.
go back to reference Patel P, Mandal A, Gote V, Pal D, Mitra AK (2019) Thermosensitive hydrogel-based drug delivery system for sustained drug release. J Polym Res 26(6):131CrossRef Patel P, Mandal A, Gote V, Pal D, Mitra AK (2019) Thermosensitive hydrogel-based drug delivery system for sustained drug release. J Polym Res 26(6):131CrossRef
29.
go back to reference Sethia S, Squillante E (2004) Solid dispersion of carbamazepine in PVP K30 by conventional solvent evaporation and supercritical methods. Int J Pharm 272(1–2):1–10CrossRef Sethia S, Squillante E (2004) Solid dispersion of carbamazepine in PVP K30 by conventional solvent evaporation and supercritical methods. Int J Pharm 272(1–2):1–10CrossRef
Metadata
Title
Preparation and in vitro characterization of polyvinylpyrrolidone-poloxamer polymeric synergy for oral drug delivery
Authors
Saman Ali
Abid Mehmood Yousaf
Syed Atif Raza
Yasser Shahzad
Ikram Ullah Khan
Tariq Mahmood
Talib Hussain
Mobina Manzoor
Humayun Riaz
Muhammad Jamshaid
Publication date
01-07-2019
Publisher
Springer Netherlands
Published in
Journal of Polymer Research / Issue 7/2019
Print ISSN: 1022-9760
Electronic ISSN: 1572-8935
DOI
https://doi.org/10.1007/s10965-019-1839-9

Other articles of this Issue 7/2019

Journal of Polymer Research 7/2019 Go to the issue

Premium Partners