Recent advances in natural small molecules as drug delivery systems

被引:20
作者
Fu, Shiyao [1 ,2 ]
Yang, Xin [1 ,2 ,3 ]
机构
[1] Harbin Inst Technol, Sch Med & Hlth, 92,West Dazhi St, Harbin 150001, Peoples R China
[2] Harbin Inst Technol, Sch Chem & Chem Engn, 92,West Dazhi St, Harbin 150001, Peoples R China
[3] Harbin Inst Technol, Chongqing Res Inst, 188 Jihuayuan South Rd, Chongqing 401135, Peoples R China
基金
中国国家自然科学基金;
关键词
SYNERGISTICALLY ENHANCED ANTITUMOR; OLEANOLIC ACID NANOSUSPENSIONS; PI-PI STACKING; BETULINIC ACID; IN-VITRO; ANTICANCER ACTIVITY; CANCER-TREATMENT; NANOPARTICLES; PRODUCTS; NANOMEDICINES;
D O I
10.1039/d3tb00070b
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
Drug delivery systems (DDSs) are a multidisciplinary approach toward the effective delivery of drugs to their target sites. Natural small molecule (NSM) compounds with anticancer activity, self-assembly and co-assembly functions show great potential for application as novel DDSs in the biomedical field. NSMs are widely sourced, have many modification sites, and readily form hydrogen bonds, pi-pi interactions, van der Waals interactions, and other non-covalent bonds in solvents, resulting in ordered structures. Moreover, their good biocompatibility and bioactivity allow compositions based on these compounds to be used in life science applications such as tissue engineering, drug delivery and cell imaging, showing the potential medical value of NSMs as DDSs. In this review, we summarise the role, assembly principles and applications of natural products such as triterpenoids, diterpenoids, sterols, alkaloids and polysaccharides in the construction of small molecule systems, which are expected to provide an important reference for the development of more active natural nanomaterials and the study of single or multi-component interactions.
引用
收藏
页码:4584 / 4599
页数:17
相关论文
共 156 条
  • [1] Isolation and evaluation of anticancer efficacy of stigmasterol in a mouse model of DMBA-induced skin carcinoma
    Ali, Huma
    Dixit, Savita
    Ali, Daoud
    Alqahtani, Saeed M.
    Alkahtani, Saad
    Alarifi, Saud
    [J]. DRUG DESIGN DEVELOPMENT AND THERAPY, 2015, 9 : 2793 - 2800
  • [2] Alla M., 2022, MOLECULES, V27
  • [3] Vesicular self-assembly of a natural ursane-type dihydroxy-triterpenoid corosolic acid
    Bag, Braja G.
    Garai, Chhabi
    Ghorai, Subrata
    [J]. RSC ADVANCES, 2019, 9 (27) : 15190 - 15195
  • [4] First Vesicular Self-Assembly of Crotocembraneic Acid, a Nano-Sized Fourteen Membered Macrocyclic Diterpenic Acid
    Bag, Braja G.
    Barai, Abir C.
    Wijesekera, Kanchana
    Kittakoop, Prasat
    [J]. CHEMISTRYSELECT, 2017, 2 (17): : 4969 - 4973
  • [5] Self-assembly of naturally occurring stigmasterol in liquids yielding a fibrillar network and gel
    Bag, Braja Gopal
    Barai, Abir Chandan
    [J]. RSC ADVANCES, 2020, 10 (08) : 4755 - 4762
  • [6] Self-assemblyofRenewable Nano-sized Triterpenoids
    Bag, Braja Gopal
    Majumdar, Rakhi
    [J]. CHEMICAL RECORD, 2017, 17 (09) : 841 - 873
  • [7] Nanoarchitectures by hierarchical self-assembly of ursolic acid: entrapment and release of fluorophores including anticancer drug doxorubicin
    Bag, Braja Gopal
    Das, Subhajit
    Hasan, Sk Nurul
    Barai, Abir Chandan
    [J]. RSC ADVANCES, 2017, 7 (29): : 18136 - 18143
  • [8] Hierarchical Self-Assembly of a Renewable Nanosized Pentacyclic Dihydroxy-triterpenoid Betulin Yielding Flower-Like Architectures
    Bag, Braja Gopal
    Dash, Shib Shankar
    [J]. LANGMUIR, 2015, 31 (51) : 13664 - 13672
  • [9] Vesicular and Fibrillar Gels by Self-Assembly of Nanosized Oleanolic Acid
    Bag, Braja Gopal
    Paul, Koushik
    [J]. ASIAN JOURNAL OF ORGANIC CHEMISTRY, 2012, 1 (02) : 150 - 154
  • [10] Self-assembly of a renewable nano-sized triterpenoid 18β-glycyrrhetinic acid
    Bag, Braja Gopal
    Majumdar, Rakhi
    [J]. RSC ADVANCES, 2012, 2 (23): : 8623 - 8626