Nose-to-brain delivery of nano-engineered biomaterials for effective targeting to the brain

被引:0
作者
Kashif, Mehboob Ur Rehman [1 ,2 ]
Sohail, Muhammad [1 ,3 ]
Mahmood, Arshad [4 ,5 ]
Shah, Syed Ahmed [6 ,7 ]
Abbasi, Mudassir [1 ,8 ]
Kousar, Mubeen [1 ]
机构
[1] COMSATS Univ, Dept Pharm, Islamabad, Pakistan
[2] Mukabbir Coll Pharm, Gujrat, Punjab, Pakistan
[3] Cyprus Int Univ, Fac Pharm, Nicosia, Cyprus
[4] Al Ain Univ, Coll Pharm, Abu Dhabi, U Arab Emirates
[5] Al Ain Univ, AAU Hlth & Biomed Res Ctr, Abu Dhabi, U Arab Emirates
[6] Polish Acad Sci, Inst Fundamental Technol Res, Dept Biosyst & Soft Matters, Warsaw, Poland
[7] Super Univ, Dept Pharmaceut Sci, Lahore, Pakistan
[8] Univ Chenab, Dept Pharm, Gujrat, Punjab, Pakistan
关键词
Biodegradable polymers; controlled delivery; nose-to-brain delivery; polymeric nanoparticles; self-assembling micelles; thermoresponsive hydrogels; IN-SITU GEL; SOLID LIPID NANOPARTICLES; HYALURONIC-ACID; DRUG-DELIVERY; INJECTABLE HYDROGEL; PHYSICOCHEMICAL PROPERTIES; POLYMERIC NANOPARTICLES; ANTIMICROBIAL ACTIVITY; SILVER NANOPARTICLES; INTRANASAL DELIVERY;
D O I
10.1080/00914037.2024.2383412
中图分类号
TB3 [工程材料学]; R318.08 [生物材料学];
学科分类号
0805 ; 080501 ; 080502 ;
摘要
Thermoresponsive hydrogels provide a platform for sustained delivery of nanoparticles via nose-to-brain route by resisting mucociliary clearance to the enhanced mean residence time (MRT) of the formulation in the nasal cavity overcoming neurotoxicity induced by uncontrolled delivery of nanoparticles and accumulation in the brain when delivered alone. The reported study presents the synthesis of pullulan (PLN) based nanoparticles (PNP-EHBr) loaded with eletriptan hydrobromide (EHBr) via ionic gelation method having size between 26.65 nm and 29.59 nm after stability studies of 4 h incubation with an average zeta potential of 22.5 +/- 0.1 mV and entrapment efficiency of 92.048%. F-127/F-68 based hyaluronic acid-co-pectin hydrogels of EHBr-loaded PLN nanoparticles thermoresponsive hydrogels (HAP-PNP-EHBr/T-Hg) were characterized via Fourier transform infrared spectroscopy (FTIR), X-ray diffraction, thermal analysis (TGA/DSC), and scanning electron microscopy and evaluated for their gelation time, gelation temperature, gel strength, cloud point, sol-gel fraction, ex-vivo permeation, etc. HAP-PNP-EHBr/T-Hg showed drug release in a controlled pattern in both phosphate-buffered saline (PBS) and simulated nasal fluid (SNF) i.e., 90.12 and 87.99, respectively, over 48 h, while PNP-EHBR, 99.44 and 97.53 in PBS and SNF, respectively, over 8 h. The controlled release and absorption of EHBr from HAP-PNP-EHBr/T-Hg and PNP-EHBr was estimated by an in-vivo pharmacokinetic study using high-performance liquid chromatography, MRT and area under the curve (AUC) were increased up to 11.337 +/- 0.32 h and 3,104.73 +/- 75.841 ng/mL*h, 11.088 +/- 0.177 h and 3,906.64 +/- 152.86 ng/mL*h in brain and blood respectively after IN administration. This work demonstrates the successful synthesis of a twofold drug delivery system with PLN-based nanoparticles (PNP-EHBr) loaded with EHBr laden F-127/F-68 based hyaluronic acid-co-pectin hydrogels (HAP-PNP-EHBr/T-Hg).
引用
收藏
页码:899 / 922
页数:24
相关论文
共 133 条
[1]   Bioinspired sodium alginate based thermosensitive hydrogel membranes for accelerated wound healing [J].
Abbasi, Asma Riaz ;
Sohail, Muhammad ;
Minhas, Muhammad Usman ;
Khaliq, Touba ;
Kousar, Mubeen ;
Khan, Shahzeb ;
Hussain, Zahid ;
Munir, Abubakar .
INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES, 2020, 155 :751-765
[2]   Formulation strategies to modulate drug release from poloxamer based in situ gelling systems [J].
Abdeltawab, Hani ;
Svirskis, Darren ;
Sharma, Manisha .
EXPERT OPINION ON DRUG DELIVERY, 2020, 17 (04) :495-509
[3]  
Abu-Thabit NY, 2018, WOODH PUBL SER BIOM, P3, DOI 10.1016/B978-0-08-101997-9.00001-1
[4]   Chitosan based thermosensitive injectable hydrogels for controlled delivery of loxoprofen: development, characterization and in-vivo evaluation [J].
Ahmad, Umair ;
Sohail, Muhammad ;
Ahmad, Mahmood ;
Minhas, Muhammad Usman ;
Khan, Shahzeb ;
Hussain, Zahid ;
Kousar, Mubeen ;
Mohsin, Sabeeh ;
Abbasi, Mudassir ;
Shah, Syed Ahmed ;
Rashid, Haroon .
INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES, 2019, 129 :233-245
[5]   In situ gelling systems based on Pluronic F127/Pluronic F68 formulations for ocular drug delivery [J].
Al Khateb, Kosai ;
Ozhmukhametova, Elvira K. ;
Mussin, Marat N. ;
Seilkhanov, Serzhan K. ;
Rakhypbekov, Tolebai K. ;
Lau, Wing Man ;
Khutoryanskiy, Vitaliy V. .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2016, 502 (1-2) :70-79
[6]   Intranasal drug delivery of didanosine-loaded chitosan nanoparticles for brain targeting; an attractive route against infections caused by aids viruses [J].
Al-Ghananeem, Abeer M. ;
Saeed, Hayder ;
Florence, Rebecca ;
Yokel, Robert A. ;
Malkawi, Ahmad H. .
JOURNAL OF DRUG TARGETING, 2010, 18 (05) :381-388
[7]  
am Ende M T, 1997, Pharm Biotechnol, V10, P139
[8]   Permeability issues in nasal drug delivery [J].
Arora, P ;
Sharma, S ;
Garg, S .
DRUG DISCOVERY TODAY, 2002, 7 (18) :967-975
[9]   Cytotoxicity and internalization of Pluronic micelles stabilized by core cross-linking [J].
Arranja, Alexandra ;
Schroder, Andre P. ;
Schmutz, Marc ;
Waton, Gilles ;
Schosseler, Francois ;
Mendes, Eduardo .
JOURNAL OF CONTROLLED RELEASE, 2014, 196 :87-95
[10]   Nasal-Ocular Reflexes and Their Role in the Management of Allergic Rhinoconjunctivitis With Intranasal Steroids [J].
Baroody, Fuad M. ;
Naclerio, Robert M. .
WORLD ALLERGY ORGANIZATION JOURNAL, 2011, 4 :S1-S5