1,2,3,4School of Pharmacy, Abhilashi University, Chail-Chowk, Himachal Pradesh, India 175028.
5School of Pharmacy, Vidya University, Meerut, Uttar Pradesh, India 250002.
Impatiens glandulifera belongs to family Balsaminaceae. It is found in the foothills of the western Himalaya, i.e. India, Pakistan, Nepal and also in European countries. Different parts of the plant has been used to treat various ailments. It is effective in joint pain. Plant seeds are chewed or seed oil is used as tonic and for the treatment of anxiety. The root extract or paste made from roots are applied to cool hands and feet. Roots, leaves and flowers powders and decoctions are used for depression and hypnosis. It is very good antidote for snake bites. Paste of leaves is applied externally to treat burns. The infusion from flowers is used for eye washes. Flowers are used as cathartic, diuretic, and emetic. Impatiens glandulifera has been reported to have anti-oxidant, anti-microbial, anti-proliferative, anti-cancer activity and also effective for some nervous system disorders. The main phytoconstituents found in plant are flavonoids, quinones, terpenes, sterols, coumarins, fatty acids, volatile compounds, essential oils.
Pl?nts h?v? s?rv?d ?s found?tion?l ?ill?rs within glob?l tr?dition?l m?di??l systems, driving ?h?rm???uti??l innov?tion th?t ?ontinu?s to sh??? mod?rn th?r???uti?s. N?tur?l ?om?ounds ?nd th?ir d?riv?tiv?s ?urr?ntly ?onstitut? ov?r 50% of th?r???uti? m?di??tions, und?rs?oring th?ir ?nduring r?l?v?n??.[1] Indi?’s ?ion??ring rol? in ?dv?n?ing indig?nous m?di?in?l systems m?rits em?h?sis, with min?r?l ?nd ?l?nt-d?riv?d formul?tions remaining int?gr?l to dis??s? m?n?gem?nt. Not?bly, th? glob?l r?surg?n?? of alt?rn?tiv? m?di?in? r?fl??ts ?volving st?k?hold?r alignm?nt with holisti? ??r? ??r?digms.[2] Impatiens glandulifera is a herb that belongs to family Balsaminaceae. It is having ?r??t stem (5−50 mm di?m?t?r, 1–2.5 m height) f??tur?s hollow ?or? with ??ri?h?r?l lignifi?d v?s?ul?r tissu?, whil? root system ?ombin? ?ylindri??l ?rim?ry roots (2–4 mm) with 146 ± 35 ?dv?ntitious roots (15−20 ?m l?ngth). Flow?rs demonstr?t? ?hrom?ti? v?ri?bility (purple/pink/white), ?om?lem?nt?d by distin?tiv? fiv?-?ngl?d fruit ???sul?s (1.5–5 ?m × 0.4–1.5 ?m) (Fig. 1b). Arr?ng?d in whorls of 2–5, th? l?n??ol?t?-ov?t? l??v?s (5−18 ?m × 2.5−7 ?m) ??hibit 18–50 s?rr?tions ??r m?rgin ?nd ??umin?t? ??i??s (Fig. 1?). Th? extrafloral purple b?s?l n??t?ri?s are ?ot?nti?l r?s?rvoirs of n??hthoquinon?s th?t w?rr?nt furth?r ?hyto?hemi??l ?n?lysis. S??d mor?hology r?v??ls ??l? gr?y-brown to black ov?l-globos? stru?tur?s (3–7 mm × 2–5 mm × 1–2 mm) with rugos? ?o?ts (Fig. 1d).[3,4]
Fig. 1. Impatiens glandulifera’s morphology.
A Whole plant, b. Detail of flower and capsules, c. Leaves, d. Seeds
Plant Taxonomy
Kingdom : Plantae
Phyllum : Magnoliophyta
Class : Magnoliopsida
Order : Geraniales
Family : Balsaminaceae
Genus : Impatiens
Species : Impatiens glandulifera
Geographical Distribution
Im??ti?ns gl?ndulif?r? distribution spans P?kist?n’s north??st, Indi?’s J?mmu ?nd K?shmir, Him??h?l Pr?d?sh, Utt?r?kh?nd r?gions, N???l’s w?st?rn t?rritori?s ?nd s?l??tive Euro???n zon?s at an elevation of 2000-4000 m. The morphology ?n?bl? ?rolif?r?tion ??ross urb?n l?ndfills, for?st ?l??rings,[3,4]
Preliminary Phytocheical Screening
Preliminary phytochemical screening was perfermed on ethanolic extract of Impatiens glandulifera. The secondary metabolites that are present in the plant are enlisted in Table 1.
Table 1: Various secondary metabolites identified in Impatiens glandulifera[5]
Sr. No. |
Constituents |
Test |
Result |
1 |
Phenolic acids & Tannins |
Ferric Chloride Test |
+ve |
2 |
Flavonoids |
Lead Acetate Test |
+ve |
3 |
Quinones |
Borntrager Test |
+ve |
4 |
Coumarin |
Sodium Hydroxide Test |
+ve |
5 |
Steroids & Terpenoids |
Libermann-Burchard test |
+ve |
6 |
Glycosides |
Sulphuric Acid Test |
+ve |
7 |
Proteins |
Millon’s Test |
+ve |
8 |
Carbohydrates |
Fehling Test |
+ve |
9 |
Amino acids |
Ninhydrin test |
-ve |
Test for tyrosine |
-ve |
||
Test for cysteine |
-ve |
||
10 |
Alkaloids |
Mayer’s Test |
-ve |
Phytochemistry
The phytochemical composition of Impatiens glandulifera includes a variety of bioactive compounds found in different parts of the plant, including leaves, flowers, aerial parts, roots, stems, seed oil, their structures are compiled in Table 2. Flavonoids such as kaempferol, astragalin, quercetin, isoquercitrin, hyperoside (Fig. 2-6) and their glycosides are predominantly present in leaves, flowers and aerial parts contributing to antioxidant, anti-inflammatory and potential anticancer properties. Phenolic acids like caffeic acid, cinnamic acid, gallic acid, salicylic acid, and vanillic acid (Fig. 7-11) are widely distributed in flowers, roots and leaves playing crucial roles in plant defense and offering antimicrobial, anti-inflammatory and antioxidant benefits. Naphthoquinones such as 2-methoxy-1,4-naphthoquinone and 2-hydroxy-1,4-naphthoquinone (Fig. 12 & 13) are found in flowers, leaves and stems, known for their antimicrobial activities. Various fatty acids, including palmitic acid, stearic acid, linolenic acid and arachidic acid (Fig. 14-17) are abundant in seed oil and flower stalks, playing essential roles in plant metabolism and exhibiting potential health benefits such as anti-inflammatory and cardioprotective agent. The herb and roots contain significant volatile compounds such as α-terpinyl acetate, linalool, borneol, β-phellandrene, butylphthalide and ligustilide (Fig. 18-23) which are known for their aromatic properties and potential therapeutic effects, including sedative, antispasmodic actions. Additionally, carbohydrates like glucose, galactose, xylose and arabinose (Fig. 24-27) are found in the aerial parts and roots, essential for energy storage and structural functions. Other unique bioactive compounds such as α-spinasterol (Fig. 28), glanduliferins A and B and parinaric acid (Fig. 29) contribute to various pharmacological activities, including anti-inflammatory and antioxidant. The presence of diverse secondary metabolites suggests the plant's significant medicinal potential, supporting its traditional and modern therapeutic applications. [6, 7, 8, 9]
Table 2: Structure of Phycochemicals
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Fig. 2 Kaempferol |
Fig. 3 Astragalin |
Fig. 4 Quercetin |
Fig. 5 Isoquercitrin |
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Fig. 6 Hyperoside |
Fig. 7 Caffeic acid |
Fig. 8 Cinnamic acid |
Fig. 9 Gallic acid |
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Fig. 10 Salicylic acid |
Fig. 11 Vanillic acid |
Fig. 12 2-Methoxy-1,4-naphthoquinone |
Fig. 13 2-Hydroxy-1,4-naphthoquinone |
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Fig. 14 Palmitic acid |
Fig. 15 Stearic acid |
Fig. 16 Linolenic acid |
Fig. 17 Arachidic acid |
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Fig. 18 α-Terpinyl acetate |
Fig. 19 Linalool |
Fig. 20 Borneol |
Fig. 21 β-Phellandrene |
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Fig. 22 Butylphthalide |
Fig. 23 (Z)-Ligustilide |
Fig. 24 Glucose |
Fig. 25 Galactose |
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Fig. 26 Xylose |
Fig. 27 Arabinose |
Fig. 28 α-Spinasterol |
Fig. 29 Parinaric acid |
Ethnopharmacological Activities
I. gl?ndulif?r? demonstr?t?s th?r???uti? ?ffi???y in joint ??in m?n?gem?nt. As both ? g?n?r?l toni? ?nd t?rg?t?d tr??tm?nt, s??ds ?r? ?h?w?d to ?ddr?ss ?n?i?ty ?nd joint dis?omfort. Through st?nd?rdiz?d ?r???r?tion m?thods, ?owd?red roots/l??v?s/flow?r d??o?tions fun?tion ?s ?sy?hotro?i? ?djuv?nts ?nd v?nom ?ount?rm??sur?s. E?t?rn?l ???li??tion of l??v?s show good results in burn rem?di?tion. O?hth?lmi? solutions d?riv?d from flor?l infusions demonstr?t? s?nitizing ?ro??rti?s. Th? s???i?s' blossoms ?r? furth?r em?loy?d in ?rthr?lgi? mitig?tion ?longsid? ?urg?tiv?, em?ti? and diur?ti? int?rv?ntions. Flow?rs are also incorporated into sn?k?bit? ?ntidot?s. L??f-b?s?d ?r???r?tions ?rovid? lo??liz?d ?ooling through ??id?rm?l ???li??tion. Nutrition?l utiliz?tion ??tt?rns ?onfirm th? ?l?nt's fruits, s??ds, foli?g? and stems ?s vi?bl? di?t?ry ?om?on?nts.[10]
Biological Activity
Antioxidant activity
Thr?? ??tr??tion mod?liti?s—So?hl?t, ultr?sound-?ssist?d, ?nd ????l?r?t?d solv?nt w?r? system?ti??lly ?om??red for ?h?noli? ??id r??ov?ry from I. gl?ndulif?r? flor?l and v?g?t?tiv? tissu?s. O??r?tion?l ??r?m?t?rs (80-120°C, 100 b?r) ?rodu??d TPAC v?lu?s of 188.07-281.82 µg/mL, with So?hl?t-d?riv?d flow?r ??tr??ts ??hibiting ???k DPPH n?utr?liz?tion (IC50 0.06 mg/mL). HPLC-ESI–MS/MS ?rofiling id?ntifi?d ?roto??t??hui? ??id ?s th? domin?nt ?onstitu?nt, ???om??ni?d by gentilic acid, trans-caffeic acid, vanillic acid, p-hydroxybenzoic acid, syringic acid, p-coumaric acid, salicylic acid, cis-ferulic acid, cis-caffeic acid, gallic acid and 3-hydroxy cinnamic acid as ?n?ill?ry ?h?noli? ??ids showing tissu?-s???ifi? distribution ??tt?rns.[7] M?th?nol ??tr??tion of ??ri?l ??rts yi?ld?d 2-methoxy-1,4-naphthoquinone, aempferol 3-O-glucoside (astragalin), quercetin 3-O-glucoside (isoquercetin), kaempferol 3-O-rutinoside (nicotiflorin), kaempferol 3-O-rhamnosyldiglucoside, p-hydroxybenzoic acid, protocatechuic acid, kaempferol 3-O-galactoside (trifolin), hyperoside, eriodictyol, and eriodictyol 7-O-β-D-glucoside ?h?noli? ?om?ounds, th?ir ?ntio?id?nt ?ot?nti?l qu?ntifi?d through du?l r?di??l ?ss?ys. Isoqu?r??tin em?rg?d ?s th? most ?ot?nt ?g?nt, demonstr?ting IC50 v?lu?s of 0.11 mg/mL (DPPH) ?nd 0.01 mg/mL (ATBS). This ?om?ound ?lust?r in?luding hy??rosid? ?nd ?riodi?tyol d?riv?tiv?s highlights th? s???i?s' div?rs? ?hyto?hemi??l r???rtoir?.[8] Ess?nti?l oil hydrodistill?tion from ??ri?l stru?tur?s ?rodu??d sup?rior ?ntio?id?nt out?om?s v?rsus root-d?riv?d ?quiv?l?nts, ?vid?n??d by DPPH IC50 3.96 µg/mL ?nd linol?i? ??id inhibition ?t 102.08 µg/mL. GC-MS ?n?lysis of th? 0.22% w/yi?ld oil id?ntifi?d β-?h?ll?ndr?n? (7.4%) ?nd α-t?r?inyl ???t?t? (16.6%) ?s m?jor ?onstitu?nts, with ?rom?ti? vol?til?s ?om?rising 23% of th? tot?l ?hyto?om?l??.[9] An?lysis r?v??l?d ?ronoun??d ?ntio?id?nt ??tivity in ?st?rifi?d fr??tions from I. gl?ndulif?r? s??d, l??f ?nd root ??tr??ts. Not?bly, DPPH r?di??l s??v?nging ?ffi???y w?s most ?ronoun??d in th? l??f-d?riv?d f?tty ??id fr??tion (IC50 11.69 µg/mL), with m?t?l ?h?l?tion ?????ity ???king ?t IC50 5.49 µg/mL. GC-MS/FID qu?ntifi??tion id?ntifi?d α-linol?ni? ??id domin?n?? (40.5%) within this bio??tiv? ?rofil?.[11] Polys???h?rid? ??tr??tion m?thodologi?s w?r? o?timiz?d through hydro?l?oholi? m???r?tion ?nd ultr?sound-?ssist?d t??hniqu?s. GC-FID ?h?r??t?riz?tion demonstr?t?d g?l??turoni? ??id ?s th? ?rim?ry monos???h?rid? ??ross Im??ti?ns s???i?s, with I. gl?ndulif?r? yi?lding m??im?l ?on??ntr?tions. Subs?qu?nt in-vitro ?v?lu?tion ?onfirm?d sup?rior ?ntio?id?nt ??rform?n?? in th?s? ?olys???h?rid? m?tri??s.[12]
Anti-inflammatory and analgesic activities
R?s??r?h?rs isol?t?d ?olys???h?rid?s from ??ri?l ??rts ?nd roots of I. gl?ndulif?r?, demonstr?ting ? 32.7% redu?tion in IL-8 ???r?ssion within LPS-stimul?t?d hum?n n?utro?hils ?t 50 µg/mL ?on??ntr?tions during in vitro t?sting. Cytoto?i?ity ?ss?ssm?nts r?v??l?d no ?dv?rs? ?ff??ts on ??ll vi?bility ?t this dos?g?, ?onfirming bio?om??tibility.[12] Th? findings sugg?st o?timiz?d th?r???uti? ?ot?nti?l through t?rg?t?d infl?mm?tory ??thw?y modul?tion.
Antimicrobial activity
An?lysis r?v??ls th? ??ri?l ??rts ??tr??t of Im??ti?ns gl?ndulif?r? ??hibit?d no m??sur?bl? im???t on Gr?m-n?g?tiv? b??t?ri?l growth. Antib??t?ri?l ?ffi???y ?g?inst Gr?m-?ositiv? ??thog?ns was demonstr?t?d through ?g?r dilution t?sting, t?rg?ting S. ?ur?us, S. ??id?rmidis, M. lut?us, B. subtilis, B. ??r?us, Str. ?n?umoni??, ?nd Str. ?yog?n?s. Bro?d-s???trum ?ntimi?robi?l ??tivity ?h?r??t?riz?s I. gl?ndulif?r?, with o??r?tion?l thr?sholds r?v??ling str?t?gi? ?ot?nti?l. Minimum inhibitory ?on??ntr?tions r?ng?d from 250 to 1000 µg/ml ??ross r?f?r?n?? str?ins, findings sugg?sting mild to mod?r?t? bio??tivity gr?di?nts.[13]
Antineoplastic activity
Ph?rm??ologi??l ?rofiling of I. gl?ndulif?r? s??d d?riv?tiv?s r?v??l?d trit?r??noid fr??tions from ??trol?um ?th?r ??tr??ts (45-60°C) ??hibit?d height?n?d ?ffi???y ?g?inst HL-60 ?nd HL-60/MX2 l?ukemi? models, dis?l?ying IC50 r?ng?s from 11.69-88.07 µg/mL. Chrom?ti? ?n?lysis ?onfirm?d α-s?in?st?rol ???t?t? ?s th? domin?nt ?om?ound within th?s? bio??tiv? fr??tions, ?onstituting 21.63% of th? isol?t?d m?t?ri?l.[11] Cytoto?i?ity ?v?lu?tions demonstr?t?d ?nh?n??d ??tivity in ?thyl ???t?t? stem ??tr??ts from I. gl?ndulif?r? ??ross A-549, U373, ?nd SMEL-28 ??ll lines, with stem-d?riv?d m?t?ri?l showing sup?rior ?ot?n?y (m?di?n IC50 33 μg/mL). Two k?y ?hyto?onstitu?nts—2-m?tho?y-1,4-n??hthoquinon? ?nd s?in?st?rol w?r? isol?t?d through t?rg?t?d fr??tion?tion of stems, l??v?s, ?nd roots. Also, gl?ndulif?rin A ?nd B w?r? uniqu?ly id?ntifi?d in stem ??tr??ts. Ag?inst SMEL-28 m?l?nom? lines, 2-m?tho?y-1,4-n??hthoquinon? em?rg?d ?s th? ?rim?ry ?ytoto?i? ?g?nt, ??hi?ving IC50 v?lu?s b?tw??n 2-3 µg/mL.[14]
This ?r?s?nts ?n o??ortunity to ???lor? stru?tur?-??tivity r?l?tionshi?s within th? trit?r??noid class for th?r???uti? d?v?lo?m?nt.
Antidepressant and anxiolytic activities
Proto??t??hui? ??id ?nd hy??rosid?, isol?t?d from I. gl?ndulif?r?'s ?th?noli? ??tr??t demonstr?t?d ?ntid??r?ss?nt ?ffi???y in Albino Swiss mi??. Immobility tim? d??r??s?d signifi??ntly ?t 1.875 mg/kg intr???riton??l dos?s during Forced Swim Test ?nd Tail Suspension Test ?v?lu?tions. The hi??o??m??l Brain Derived Neurotrophic Factor l?v?ls in?r??s?d subst?nti?lly ?t ?l?v?t?d dos?s of 3.75 mg/kg ?nd 7.5 mg/kg. This m??h?nism ?????rs ??ntr?l to th? obs?rv?d n?uror?gul?tory ?ff??ts, with BDNF u?r?gul?tion s?rving ?s ? ?rob?bl? m??h?nisti? ??thw?y for mood disord?r rem?di?tion.[15]
CONCLUSION
The plant Impatiens glandulifera consist a variety of phytoconstituents. Since much research work has not been done on plant and very less literature is available. The studies exhibit the different type of compounds like flavonoids, glycosides, phenolics, phytosterols, triterpenoids, peptides and activities that has been reported, antioxidant, cytotoxic, antimicrobial, analgesic, anti-inflammatory, antidepressant and anxiolytic effects are the most frequent. Ethnobotanical information can guide to explore this plant for phytoconstituents and pharmacological screening and to make use of this plant in vivo pharmacological study may be conducted. It is concluded that the plant is of many uses.
Abbreviations
MIC |
Minimum Inhibitory Concentration |
IC |
Inhibitory Concentration |
LPS |
Lipopolysaccharides |
GC-FID |
Gas Chromatography with Flame Ionization Detector |
GC-MS |
Gas Chromatography Mass Spectrometry |
ATBS |
2,2′-azino-bis(3-ethylbenzothiazoline-6-sulfonic acid) |
DPPH |
2,2-diphenyl-1-picrylhydrazyl |
REFERENCES
Dev Prakash Dahiya, Bhavneshwari Devi*, Shivani, Anchal Sankhyan, Nishant Verma, A Review on Himalayan Balsam (Impatiens Glandulifera), Int. J. of Pharm. Sci., 2025, Vol 3, Issue 4, 273-280 https://doi.org/10.5281/zenodo.15126683