Alginate and Chitosan-Based Delivery Systems for Improving the Bioavailability and Therapeutic Efficacy of Curcumin

被引:8
作者
Sable, Anand A. [1 ,2 ]
Kunwar, Amit [1 ,2 ]
Barik, Atanu [1 ,2 ]
机构
[1] Bhabha Atom Res Ctr, Radiat & Photochem Div, Mumbai 400085, India
[2] Homi Bhabha Natl Inst, Mumbai 400094, India
关键词
curcumin; drug delivery system; nano-formulation; alginate; chitosan; DRUG-DELIVERY; SODIUM ALGINATE; NANOPARTICLES; DEMETHOXYCURCUMIN; NANOCARRIERS; ANTIOXIDANT; DERIVATIVES; CHEMISTRY; MICELLES;
D O I
10.3390/pharmaceutics16030423
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
One of the major challenges in harnessing the therapeutic benefits of curcumin (an active ingredient from turmeric) is its poor bioavailability due to its short biological half-life. In this regard, nanoformulations have shown tremendous hope for improving the pharmacokinetic and therapeutic behavior of curcumin by altering its biological stability and bioavailability. Biopolymers, especially alginate and chitosan, have received special attention as excipients to prepare nanoformulations of curcumin due to their abundant availability, biocompatibility, and amicability to form different types of self-assembled structures and ease of undergoing chemical modifications. However, there are certain challenges, such as poor water solubility under physiological conditions and heterogeneity with regard to molecular weight and large-scale production of well-preserved nanostructures. Substantial advancement has been achieved towards overcoming these challenges by developing newer derivatives through a chemical modifications approach, and this has ascertained the suitability of alginate and chitosan as excipients for drug delivery systems (DDS). The present minireview briefly discusses curcumin and its limitation as a drug molecule, carbohydrates as DDS, and the recent developments related to the alginate and chitosan-based nanoformulations of curcumin. Special emphasis has been given to highlighting the impact of alginate and chitosan-based nanoformulations in improving the therapeutic efficacy and bioavailability of curcumin.
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页数:16
相关论文
共 84 条
[1]   Alginate as a Promising Biopolymer in Drug Delivery and Wound Healing: A Review of the State-of-the-Art [J].
Abourehab, Mohammad A. S. ;
Rajendran, Rahul R. ;
Singh, Anshul ;
Pramanik, Sheersha ;
Shrivastav, Prachi ;
Ansari, Mohammad Javed ;
Manne, Ravi ;
Amaral, Larissa Souza ;
Deepak, A. .
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2022, 23 (16)
[2]   Controlled Drug Delivery Systems: Current Status and Future Directions [J].
Adepu, Shivakalyani ;
Ramakrishna, Seeram .
MOLECULES, 2021, 26 (19)
[3]  
Aggarwal BB, 2007, ADV EXP MED BIOL, V595, P1
[4]   Pro-oxidant, anti-oxidant and cleavage activities on DNA of curcumin and its derivatives demethoxycurcumin and bisdemethoxycurcumin [J].
Ahsan, H ;
Parveen, N ;
Khan, NU ;
Hadi, SM .
CHEMICO-BIOLOGICAL INTERACTIONS, 1999, 121 (02) :161-175
[5]   A review on chitosan and its nanocomposites in drug delivery [J].
Ali, Akbar ;
Ahmed, Shakeel .
INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES, 2018, 109 :273-286
[6]   Bioavailability of curcumin: Problems and promises [J].
Anand, Preetha ;
Kunnumakkara, Ajaikumar B. ;
Newman, Robert A. ;
Aggarwal, Bharat B. .
MOLECULAR PHARMACEUTICS, 2007, 4 (06) :807-818
[7]   Development, Characterization and Pharmacokinetic Profile of Chitosan-Sodium Tripolyphosphate Nanoparticles Based Drug Delivery Systems for Curcumin [J].
Arozal, Wawaimuli ;
Louisa, Melva ;
Rahmat, Deni ;
Chendrana, Priska ;
Sandhiutami, Ni Made Dwi .
ADVANCED PHARMACEUTICAL BULLETIN, 2021, 11 (01) :77-85
[8]   Comparative study of copper(II)-curcumin complexes as superoxide dismutase mimics and free radical scavengers [J].
Barik, Atanu ;
Mishra, Beena ;
Kunwar, Amit ;
Kadam, Ramakant M. ;
Shen, Liang ;
Dutta, Sabari ;
Padhye, Subhash ;
Satpati, Ashis K. ;
Zhang, Hong-Yu ;
Priyadarsini, K. Indira .
EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 2007, 42 (04) :431-439
[9]   Characterization of Self-Assembled Polyelectrolyte Complex Nanoparticles Formed from Chitosan and Pectin [J].
Birch, Nathan P. ;
Schiffman, Jessica D. .
LANGMUIR, 2014, 30 (12) :3441-3447
[10]  
Blanco A., 2017, Medical Biochemistry, P73, DOI DOI 10.1016/B978-0-12-803550-4.00004-5