Research Progress of Ferula ferulaeoides: A Review

Abstract

Ferula ferulaeoides (Steud.) Korov is one of the traditional ethnic medicines in Xinjiang Uygur and Kazakh of China, which mainly contains volatile oils, terpenoids, coumarins and other chemical components. Previous work has shown that F. ferulaeoides exhibited insecticide, antibacterial, antitumor properties, and so on. In this paper, the chemical composition, pharmacological activity, and quality control of F. ferulaeoides were reviewed, and the application of F. ferulaeoides in the food industry was explored, so as to provide some reference for the quality evaluation of F. ferulaeoides and its further development and utilization.

1. Introduction

Ferula is a perennial herb belonging to the genus Ferula L. in the family Apiaceae, which is an important source of resin used in folk medicine [1]. There are about 180 species in the world, mainly distributed in the Mediterranean and Central Asia [2]. Among them, there are 27 species in China, 7 of which are unique [3], mainly distributed in Xinjiang, Tibet, Qinghai, Yunnan, and other provinces [4]. Ferula plants have a long history as a medicine. Ferula was utilized to treat many diseases as early as ancient Persia, so it was called “God’s food”. Nowadays, Ferula is still an indispensable member of Chinese herbal medicine in the international market. The medicinal material of Ferula is an oil–glue–resin air-dried lump, which is isolated from the genus Ferula. It is bitter in taste and warm in nature, and has benefits for the spleen and stomach. Ferula comprises three major fractions, including resin (40–64%), gum (25%) and essential oil (10–17%). The resin fraction includes ferulic acid and its esters, coumarins, sesquiterpene coumarins, and other terpenoids. The gum contains glucose, galactose, l-arabinose, rhamnose, glucuronic acid, polysaccharides, and glycoproteins, and the volatile fraction includes sulfur-containing compounds, monoterpenes, and other volatile terpenoids [5]. Ferula ferulaeoides (Steud.) Korov is one of the genera Ferula, which is often distributed in sand dunes or gravel Artemisia deserts in Mongolia, Russia, and Kazakhstan, and mainly grows in the Gobi desert in the marginal area of Junggar, Xinjiang in China [6]. F. ferulaeoides is widely used as a substitute for medicinal Ferula in Xinjiang. Its active ingredients are mainly volatile components. It has significant pharmacological activities in the treatment of insect accumulation, meat accumulation, lumps, abdominal pain, malaria, dysentery, etc. It is mostly used clinically to treat cold pain in the heart and abdomen, chronic gastroenteritis, gastric ulcers, rheumatoid arthritis, and other diseases [7].

In recent years, F. ferulaeoides has attracted the attention of researchers at home and abroad. It has been discovered that the main chemical components of F. ferulaeoides include volatile oil, resin, gum, etc. Sesquiterpenes, coumarins, and other chemical components may be the main pharmacological active components. What is more, modern pharmacological studies have shown that F. ferulaeoides has significant pharmacological activities such as insecticidal, bacteriostatic, anti-tumor, etc. In order to further develop and utilize this national medicinal material and fully understand its research status, this paper expounds on the research status of the chemical composition, pharmacological activity, and quality control of F. ferulaeoides, and looks forward to the application of F. ferulaeoides in the food industry, with the objective of providing some reference for the quality evaluation and in-depth development and utilization of resources.

2. Chemical Constituents of F. ferulaeoides

The chemical constituents of F. ferulaeoides mainly include coumarins, sesquiterpenes, and volatile oils [8]. The coumarins are one of the characteristic components of Ferula, and they are also the first compounds isolated from Ferula. The coumarins in F. ferulaeoides are mainly in the form of sesquiterpene derivatives, and simple coumarins are relatively rare. Most of the sesquiterpene coumarins in other Ferula plants are 7-hydroxy coumarins, while F. ferulaeoides contains mainly furan coumarins. As another characteristic component of Ferulae, sesquiterpenes mainly exist in the form of esters and lactone, and a few exist in the form of ketone derivatives (

Table 1. Terpenoid Derivatives from Fructus F. ferulaeoides.

Type	No.	Compound	Formula	Molecular Weight	References
Sesquiterpene–coumarins	1	Badrakemin	C24H30O4	382	[13]
	2	Badrakemin acetate	C26H32O5	424	[13]
	3	Conferol acetates	C26H32O5	424	[13]
	4	Ferulin A	C25H33O5	413	[14]
	5	Ferulin B	C24H32O5	400	[15]
	6	Ferulin C	C25H34O5	414	[14]
	7	2,3-dihydro-7-hydroxy-2S*,3R*-dimethyl-3-[4,8-dimethyl-3(E),7-nonadienyl]-furo [3,2-c] coumarin	C24H30O4	382	[14]
	8	2,3-dihydro-7-hydroxy-2R*,3R*-dimethyl-3-[4,8-dimethyl-3(E),7-nonadienyl]-furo [3,2-c] coumarin	C24H30O4	382	[14,16]
	9	2,3-dihydro-7-hydroxy-2S*,3R*-dimethyl-3-[4-methyl-5-(4-methyl-2-furyl)-3(E)-pentenyl]-furo [3,2-c] coumarin	C24H26O5	394	[14]
	10	2,3-dihydro-7-methoxy-2S*,3R*-dimethyl-3-[4,8-dimethyl-3(E),7-nonadienyl]-furo [3,2-c] coumarin	C25H32O4	396	[15]
	11	2,3-dihydro-7-hydroxy-2S*,3R*-dimethyl-2-[4,8-dimethyl-3(E),7-nonadienyl]-furo [3,2-c] coumarin	C24H30O4	382	[15]
	12	2,3-dihydro-7-hydroxy-2R*,3R*-dimethyl-2-[4,8-dimethyl-3(E),7-nonadienyl]-furo [3,2-c] coumarin	C24H30O4	382	[15]
	13	2,3-dihydro-7-hydroxy-2S*,3R*-dimethyl-2-[4,8-dimethyl-3(E),7-nonadien-6-onyl]-furo [3,2-c] coumarin	C25H32O4	396	[15]
	14	2,3-dihydro-7-hydroxy-2S*,3R*-dimethyl-2-[4-methyl-5-(4-methyl-2-furyl)-3(E)-pentenyl]-furo [3,2-c] coumarin	C24H26O5	394	[14]
	15	2,3-dihydro-7-hydroxy-2R*,3R*-dimethyl-2-[4-methyl-5-(4-methyl-2-furyl)-3(E)-pentenyl]-furo [3,2-c] coumarin	C24H26O5	394	[14]
	16	2,3-dihydro-7-methoxy-2S*,3R*-dimethyl-2-[4,8-dimethyl-3(E),7-nonadienyl]-furo [3,2-c] coumarin	C25H32O4	396	[15]
	17	2,3-dihydro-7-methoxy-2R*,3R*-dimethyl-2-[4,8-dimethyl-3(E),7-nonadienyl]-furo [3,2-c] coumarin	C25H32O4	396	[15]
	18	2,3-dihydro-7-methoxy-2S*,3R*-dimethyl-2-[4,8-dimethyl-3(E),7-nonadien-6-onyl]-furo [3,2-c] coumarin	C25H30O5	410	[15]
	19	2,3-dihydro-7-methoxy-2S*,3R*-dimethyl-2-[4-methyl-5-(4-methyl-2-furyl)-3(E)-pentenyl]-furo [3,2-c] coumarin	C25H28O5	408	[15]
	20	(trans)-2,3-dimethyl-3-[9-hydroxymethyl-4-methyl-3E,7Z-nonadienyl]-7-hydroxy-2(3H)-furo [3,2-c] coumarin	C24H31O5	399	[15]
	21	7-hydroxy-2-[1-hydroxy-1,5,9-trimethyl-4E,8-decadienyl]-2(3H)-furo [3,2-c] coumarin	C24H31O5	399	[15]
	22	2-[1-hydroxy-1,5,9-trimethyl-4E,8-decadienyl]-7-methoxy-2(3H)-furo [3,2-c] coumarin	C25H33O5	408	[15]
	23	4,7-dihydroxy-3-[3,7,11-trimethyl-2(E),6(E),10-dodecatrienyl] coumarin	C24H30O4	382	[14]
Sesquiterpene–heteroketone compounds	24	Ferulin D	C25H32O4	396	[15]
	25	Ferulin E	C24H31O4	383	[14]
	26	2,3-dihydro-7-hydroxy-2S*,3R*-dimethyl-2-[4,8-dimethyl-3(E),7-nonadienyl]-furo [3,2-b] chromone	C24H30O4	382	[14]
	27	2,3-dihydro-7-hydroxy-2S*,3R*-dimethyl-2-[4-methyl-5-(4-methyl-2-furyl)-3(E),7-pentenyl]-furo [2,3-b] chromone	C24H26O5	394	[15]
	28	2,3-dihydro-7-hydroxy-2R*,3R*-dimethyl-2-[4-methyl-5-(4-methyl-2-furyl)-3(E),7-pentenyl]-furo [2,3-b] chromone	C24H26O5	394	[15]
	29	4-hydro-7-hydroxy-2-methyl-2-[4,8-dimethyl-3E,7-nonadienyl]-2(3H)-pyro [2,3-b] chromone	C24H31O4	383	[14]
	30	2,3-dihydro-7-hydroxy-2S*,3R*-dimethyl-2-[4,8-dimethyl-3(E),7-nonadienyl]-furo [3,2-b] chromone	C24H30O4	382	[15]
	31	2,3-dihydro-7-hydroxy-2R*,3R*-dimethyl-2-[4,8-dimethyl-3(E),7-nonadienyl]-furo[3,2-b] chromone	C24H30O4	382	[15]
Sesquiterpene–phenolic compounds	32	Dshamirone (secoammoresinol)	C23H33O3	356	[15]
	33	(4E,8E)-1-(2,4-dihydroxyphenyl)-5,9,13-trimethyl-tetradeca-4,8,12-trien-1-one	C23H32O3	356	[14]
	34	(4E,8E)-1-(2,4-dihydroxyphenyl)-2-methoxycar-bonyl-5,9,13-trimethyltetradeca-4,8,12-trien-1-one	C25H34O5	414	[14]
	35	1-(2,4-dihydroxyphenyl)-3,7,11-trimethyl-3-vinyl-6(E),10-dodecadiene-1-one	C23H32O3	356	[15]
	36	8,9-oxoisopropanyldshami-rone	C22H30O5	374	[17]
	37	Ferulaeolactone A	C24H34O6	418	[17]
	38	8-acetoxy-9-hydroxydshmirone	C24H34O5	402	[17]
	39	Ferulaeone A	C25H33O5	413	[15]
	40	Ferulaeone B	C25H37O6	433	[15]
	41	Ferulaeone C	C23H31O3	355	[15]
	42	Ferulaeone D	C23H28O4	369	[15]
	43	Ferulaeone E	C33H49O4	509	[15]
	44	Ferulaeone F	C33H49O4	509	[15]
	45	Ferulaeone G	C33H43O5	519	[15]
	46	Ferulaeone H	C38H55O5	591	[15]
	47	3-(2,4-dihydroxybenzoyl)-4S*,5R*-dimethyl-5-[4,8-dimethyl-3(E),7(E)-nonadien-1-yl] tetrahydro-2-furanone	C24H32O5	400	[15]
	48	3-(2-hydroxyl-4-methoxybenzoyl)-4S*,5R*-dimethyl-5-[4,8-dimethyl-3(E),7(E)-nonadien-1-yl] tetrahydro-2-furanone	C25H34O5	414	[15]
	49	3-(2,4-dihydroxybenzoyl)-4R*,5R*-dimethyl-5-[4,8-dimethyl-3(E),7(E)-nonadien-1-yl] tetra-hydro-2-furanone	C24H32O5	400	[15]
	50	Ferulactone A	C24H32O9	463	[18]
	51	Ferulactone B	C24H30O7	429	[18]
	52	3S*-(2,4-dihydroxybenzoyl)-4R*,5R*-dimethyl-5-(4,8-dimethyl-3(E),7(E)-nonadien-1-yl) tetrahydro-2-furanone	C24H32O5	400	[19]
	53	1-(2,4-dihydroxyphenyl)-2-hydroxy-5,9,13-trimethy1-4(E),8(E),12-tetradecatrien-1-one	C23H32O4	372	[19]
	54	1-(2,4-dihydroxyphenyl)-3,7,11-trimethyl-3-vinyl-6(E),10-dodecadiene-1,9-dione	C23H30O4	370	[19]
	55	1-(2,4-dihydroxyphenyl)-3,7-dimethyl-3-vinyl-8-(4-methyl-2-furyl)-6(E)-octen-l-one	C23H28O4	368	[15]
	56	3S*-(2,4-dihydroxybenzoyl)-4R*,5R*-dimethyl-5-[4-methyl-5-(4-methyl-2-furyl)-3(E)-penten-1-yl] tetrahydro-2-furanone	C24H28O6	412	[15]
	57	3S*-(2,4-dihydroxybenzoyl)-4R*,5S*-dimethyl-5-[4-methyl-5-(4-methyl-2-furyl)-3(E)-penten-l-yl] tetrahydro-2-furanone	C24H28O6	421	[15]

, Structures of sesquiterpenes are shown Figure 1, Figure 2 and Figure 3). The constituents of the volatile oil obtained from F. ferulaeoides have been studied more over recent years. More than 100 compounds have been separated from the volatile oil, including monoterpenes, sesquiterpenes, fatty family compounds, aromatic family compounds, and alcohol ester compounds, etc., (

Table 2. Main chemical compositions in volatile oil of F. ferulaeoides.

Type	Compound	References
Monoterpenoids	α-pinene, β-pinene, camphene, δ-3-carene, limonene, D-limonene, L-limonene, α-phellandrene, β-thujene, γ-terpinene, ocimene, β-ocimene, terpinolene, α-terpinolene, myrcene, β-myrcene, sabinene, fenchene, fenchol, borneol, (R)-camphor, citronellol, P-cymen-8-ol, α-terpined, 1,7,7-trimethyl-exo-bicyclo[2.2.1]heptan-2-ol, tanacetone, Z-3-pnen-2-ol, isogeraniol), 3-methoxy-p-cymene, dihydrocarvyl aetate, thymylether methyl, 2-camphanol acetate, exobornyl acetate, α-fenchyl acetate, [1,3,6-octatriene,3,7-dimethyl-,(Z)-], 3-isopropylidene-5-methyl-hex-4-en-2-one)	[8]
Sesquiterpene	Farnesene, α-guaiene, α-farnesene, β-farnesene, α-curcumene, β-curcumene, α-elemene, β-elemene, valencene, (−)-alloaromadendrene, trans-caryophyllene, aristolene, α-gurjunene, α-cedrene, β-cedrene, hujopsenet, α-himachalene, β-himachalene, α-bulnesene, isoledene, (Z,E)-α-farnesene, 1.2,3,4,4A,5,6,8A-octa-hydro-naphthalene, bergamotene, γ-selinene, α-bergamotene, zingiberene, isocaryophyllene, ledene, β-bisabolene, τ-guaiene, guaiol, α-guaiol, δ-guaiol, bulnesol, 10-O-γ-eudesmol, α-eudesmol, τ-eudesmol, β-eudesmol, elemiol, cedrol, hinesol, agarospirol, ginsenol, calareneexoide, eudesm-7(11)-en-4-ol, β-bisabolol, nerolidol, trans-nerolidol, 1,2- propanediol,3-methoxy-, 2,6,6-trimethyl-1- methylen-cyclohex-2-ene, 5,9-undecadien- 2-one,6,10-dimethyl-,(Z)-, 1,1-dimethyl-2,4-di(1-propenyl)cyclohexane, (Z)-2,6,10- trimethyl-1,5,9-undecatriee, 5-β-H,7-β, 10-α-selina-4(19),11-diethy, 4-(1E)-1,3-butadien-1-yl-3,5,5-trimethyl]	[8]
Aromatic	Toluene, resorcinol, O-cymene, benzene, 2-methoxy-4-vinylphenol, 1-methyl-4-(1-methylethyl) benzene, 4-(1-methylethyl)-benzene-methanol, 1-1,5-dimethyl-4- hexenyl-4-methyl benzene	[8]
Alcohol esters	cyclopentanol,2-methyl acetate, neryl acetate, butane-2,3-diol, (2S,3S)-(+)-2,3-butane diol, 4,8-dimethyl-3,7-nonadien-2-ol, 4-terpinyl acetate, α-terpinyl acetate, ethyl palmitate, ethyl linoleate	[8]

) [6,8,9]. At the same time, it also contains phenols or phenolic acids, phenylpropanoids, steroids and other compounds (

Table 3. Other chemical constituents of F. ferulaeoides.

Type	No.	Compound	Formula	Molecular Weight	References
Phenylpropanoids	1	myristicin	C11H12O3	192	[19]
Phenols, phenolic acids	2	2,4-dihydroxyacetophenone	C8H8O3	152	[19]
	3	2-hydroxy-4-methoxyacetophenone	C9H10O3	166	[19]
	4	2,4-dihydroxybenzoic acid	C7H6O4	154	[19]
	5	2,4-dihydroxy-α-oxobenzeneacetic acid	C8H8O4	168	[19]
	6	β-resorcylic acid	C7H6O4	154	[19]
	7	Methoxyresorcylic acid	C8H8O4	168	[19]
	8	Umbelliferone	C9H6O3	162	[6]
	9	Lehmannmlone	C24H30O4	382	[6]
	10	methyl 2,4-dihydroxybenzoate	C8H8O4	168	[6]
	11	ethyl 2,4-dihydroxybenzoate	C9H10O4	182	[6]
Steroids	12	β-sitosterol	C29H50O	414	[19]
	13	Daucossterol	C35H60O6	576	[6]

). In addition, polysaccharides, flavonoids, and ferulic acid are also effective components of F. ferulaeoides, but at present, there are few studies on polysaccharides and flavonoids, and they still remain in the extraction process and content determination. Currently, ultrasonic extraction and Soxhlet extraction are the most commonly used methods to extract polysaccharides and flavonoids of F. ferulaeoides [10,11]. Ferulic acid is a phenolic acid, rarely exists in free form, mainly binds with oligosaccharides, polyamines, lipids, and polysaccharides, and has antibacterial and anti-inflammatory, antioxidant, antithrombotic, and other pharmacological effects [12].

3. Pharmacological Effects of F. ferulaeoides

3.1. Antimicrobial Activity

The emergence of bacterial resistance to different classes of antibacterial agents such as β-lactams, quinolones, and macrolides is a major problem that seriously affects human health. Therefore, during the past two decades, researchers have paid great attention to the development of antimicrobial agents, especially those of a natural origin. In addition to their efficacy, most of the natural products are non-toxic, so they can be used as a safe treatment strategy [20]. Among medicinal plants, the Ferula species has been identified as a rich source of antimicrobial compounds, with a variety of Ferulic plants having antibacterial effects (

Table 4. Antibacterial Effect of Ferula Plants.

Ferula Plants	Antibacterial Ingredients	Microorganism	References
F. lycia	essential oil	Haemophilus influenza T	[23]
F. glauca	essential oil	Streptococcus mutans, Enterococcus faecalis, Escherichia coli	[23]
F. heuffelii	essential oil	Micrococcus luteus, Staphylococcus epidermidis, B. subtilis,Micrococcus flavus	[23]
F. assafoetida	organic extractswater extracts	coli, S. aureus, E. faecalis, Shigella flexneri, Klebsiella pneumonia	[21,23]
F. gummosa	oleo-resin	E. coli, P. aeruginosa, S. aureus, Salmonella enteritidis, Listeria monocytogenes	[23]
	essential oil	C. albicans, S. epidermidis, S. aureus, E. coli, B. cereus, E. faecalis, P. aeruginosa
F. communis	petroleum ether extract	S. aureus, B. subtilis, Streptococcus durans, E. faecalis	[23]
F. szovitsiana	essential oil	B. subtilis	[23]
F. hermonis	essential oil	S. typhi, P. aeruginosa, E. coli, S. aureus, S. fecalis	[23]
F. vesceritensis	essential oil	E. coli, K. pneumonia, S. aureus, P. aeruginosa	[23]
F. kuhistanica	essential oil	S. aureus	[23]
F. ferulaeoides	sesquiterpene derivatives	Drug-resistant S. aureus	[14] [22]
	alcohol extract	S. aureus, B. subtilis, Sarcina
F. elaeochytris	essential oil	S. aureus	[24]
F.pseudalliacea	sesquiterpene coumarins	S. aureus, Enterococcus faecium, B. cereus, E. coli, P. aeruginosa	[23]
F. tunetana	essential oil	Salmonella typhimurium, S. epidermidis, Micrococcus luteus, B. Cereus, B. subtilis	[25]
F. tingitana L.	essential oil	Bacillus subtilis, Neisseria gonorrhoeae	[26]

). The inhibitory effect of F. ferulaeoides on microorganisms was mainly manifested in Staphylococcus aureus, Bacillus subtilis, and Sarcina. Liu et al. isolated some terpenoid derivatives from F. ferulioides and used them in the antibacterial experiments of drug-resistant S. aureus strains including SA1199B (resistant to fluoroquinolones), XU212 (resistant to both tetracycline and methicillin), ATCC25923 (non-resistant), RN4220 (resistant to erythromycin), EMRSA15 (epidemic hospital MRSA), and EMRSA16 (epidemic hospital MRSA). These terpenoid derivatives showed obvious antibacterial activity [17,21]. Gao et al. carried out bacteriostatic tests on the extract and alcohol extract of Ferula sinkiangensis, Ferula ferulaeoides, and Ferula sinkiangensis leaves by the disc diffusion method. The results showed that the alcohol extracts of three kinds of Ferula leaves had good bacteriostatic effects on S. aureus, B. subtilis, and Eight fold aureus, among which F. ferulaeoides had the strongest inhibitory effect [22].

3.2. Antitumor Effect

In recent years, the treatment of various cancers with traditional Chinese medicine has attracted the extensive attention of scholars at home and abroad, and there is an urgent need to find safe and effective anti-tumor drugs from traditional Chinese medicine resources [27]. F. ferulaeoides is a traditional Chinese medicine in Xinjiang, and its anti-tumor research has also attracted the attention of domestic scholars. Yang et al. detected the inhibition effects of different extracts (with volatile oil, 95% ethanol extract, petroleum ether, chloroform, ethylacetate, n-butanol, and water fraction) from F. ferulaeoides on five types of gastric cancer cell lines (AGS, MKN-45, BGC-823, MGC-803 and SGC-7901). As a result, volatile oil, 95% ethanol extract and its petroleum ether, chloroform, and ethyl acetate fraction on five types of gastric cancer cells had different proliferation inhibition effects. Among them, the chloroform fraction had a good sensitivity to the five types of gastric cancer cell lines, with the highest sensitivity in the gastric cancer cell lines SGS-7901, and the volatile oil had a strong inhibitory effect on gastric cancer cell AGS [28]. Malignant peripheral-nerve sheath tumors (MPNSTs) are the sixth most common invasive soft tissue sarcoma, originating from the Schwann cell lineage or its precursors, with highly invasive properties in relation to surrounding peripheral nerves and there is currently no effective treatment. DAW22, a natural sesquiterpene coumarin isolated from F. ferulaeoides by Li et al., was found to inhibit cell proliferation and colony formation in five established human MPNST cancer cell lines, which provided strong evidence for DAW22 as a potential new alternative therapy for MPNST patients [29]. Other than that, DAW22 can induce apoptosis in C6 glioma cells occurred via the mitochondria-mediated and death-receptor pathways. It inhibited C6 glioma cell growth in a time- and concentration-dependent manner with an IC₅₀ value (at 24 h) of 18.92 μM [30]. F. ferulaeoides has also been studied in inhibiting the activity of cervical cancer cells. Ma et al. [31] studied the anti-cervical cancer activity of four kinds of ethanol extracts from Xinjiang Ferula including F. ferulaeoides. The results showed that F. syreitschikowii, F. feurlaeoides, F. akitschkensis, and F. soongarica could inhibit and promote the apoptosis of human cervical cancer Hela cells, and the apoptosis rates were 54.82%, 48.99%, 51.83% and 69.75%, respectively.

3.3. Anti-Inflammatory Effect

Researchers at home and abroad have found that Ferula has a clear anti-inflammatory effect [32]. The anti-inflammatory activity of F. ferulaeoides was studied as early as 1993. For instance, Ye et al. found that three species of Ferula including F. ferulaeoides could inhibit carrageenan-induced rat voix pedis swelling [33]. A patent in 2013 proved that ferulin A, B, C, D, and E in F. ferulaeoides have anti-inflammatory activity with effective doses in the range of 5–15 μ mol kg⁻¹ [34]. In a study completed in 2021, the researchers established the inflammation model of lipopolysaccharide (LPS)-stimulated mouse macrophages RAW264.7 and detected the content of NO by the Griess reagent method. Moreover, they conducted the correlation analysis between the NO content and HPLC spectra of different polar extracts of Ferula sinkiangensis K.M Shen, Ferula fukanensis K.M Shen, and Ferula. Ferulaeoides by bivariate Pearson correlation analysis, and screened the anti-inflammatory active extracts. The results showed that the 95% ethanol extract, methylene chloride extract, and ethyl acetate extract of three kinds of Ferula had significant anti-inflammatory activity, and F. ferulaeoides had significant anti-inflammatory activity at the retention time of 86 min [35].

3.4. Insecticidal Activity

Insecticidal active components in plants are secondary metabolites produced in the long-term co-evolution process of plants and insects, which is relatively safe to human, livestock, crops, and the ecological environment, and insects cannot easily produce resistance to them. Therefore, it meets the requirements of people for ideal pesticides [36]. The main insecticidal effects of F. ferulaeoides are sesquiterpenes guaiacol and volatile oil. Liu isolated a compound with insecticidal activity, guaiacol, from the methylene chloride extract of F. ferulaeoides root, and tested its insecticidal activity against aphids. The results verify that the killing rate of guaiacol to aphid was almost 100%. Furthermore, guaiacol has obvious killing activity on the fourth instar armyworm, third instar cabbage moth, and the housefly [37]. Oncomelania hupensis (O. hupensis) is the unique intermediate host of Schistosoma japonicum. Studies have shown that guaiacol in Ferula has a killing effect. In 2007, Li et al. initially observed that ferula had the effect of killing O. hupensis, and in 2015, Fu and Zhao further proved that the mechanism of O. hupensis was killed mainly through guaiacol affecting its esterase and glycogen [38,39]. It was detected that the essential oil of F.ferulaeoides. had a strong repellent activity against the adults of the stored pest, Tribolium castaneum, and the 2nd instar larvae of Plutella maculipennis Curtis and the 10th instar larvae of yellow mealworm [40].

3.5. Toxic Effect

The acute toxicity of volatile oil of F. ferulaeoides is low. The toxicity and death of mice were observed after the mice were given an emulsion of the volatile oil of F. ferulaeoides. The mortality of the mice was used as the index, and the median lethal dose of the volatile oil to mice was determined by the Bliss method; the LD₅₀ was 10240 mg·kg⁻¹ g [41].

4. Research on Quality Control

4.1. Traits and Microstructure

F. ferulaeoides is characterized by granular, teardrop-like or irregular lumps, with a yellow-white to dark brown surface, light internal color, soft texture, and sticky teeth. It smells similar to celery, but is stronger than celery, with a slightly bitter and pungent taste [42]. Ding et al. [43] observed spiral or reticulate ducts, non-glandular hairs, stone cells, and sub-prism of calcium oxalate in the microstructure of F. ferulaeoides powder, and found a large number of resin channels of different sizes distributed in the cross-sectional microstructure of the roots, stems, and leaves of F. ferulaeoides, with the maximum diameter up to 10 μm. The resin canal, as its name implies, refers to the secretory tissue that secretes and synthesizes resin, mainly the secretory tube. In another study, Liu et al. investigated the microstructure and ultrastructure of the secretory ducts from the perspective of development. Their research determined that the formation model of SDs in F. ferulaeoides was schizogenous and pectinase contributed to SDs’ formation, while resin production was due to the activity of organelles and cytoplasm of secretory cells [44].

4.2. Studies on Fingerprint

Chinese medicine fingerprinting technology is an effective method for evaluating the merits of Chinese medicines, identifying authenticity, distinguishing species and ensuring their consistency and stability. In addition, it is currently the most effective means for identifying drug varieties and evaluating drug quality at home and abroad [45]. At the moment, the fingerprint applied to F. ferulaeoides mainly focuses on the DNA fingerprint and GC-MS fingerprint. By comparing the results of different primer increases, Miao [46] selected 15 primers of ISSR and 15 primers of RAPD to establish a DNA fingerprint profile for F. ferulaeoides, which provides a reliable method for scientific evaluation, effective control of herb quality, and rapid and accurate identification of similar species of the same genus. Sheng et al. [47] established GC-MS fingerprints of 44 samples of essential oils of F. ferulaeoides from 8 producing areas. Twelve common peaks were established by analyzing forty-four essential oil samples of F. ferulaeoides. The GC-MS fingerprint of in vitro anti-gastric cancer active parts from F. ferulaeoides was investigated and analyzed by GC-MS and principal component analysis by Wang and colleagues. The method can characterize the whole information of the chloroform extraction part of the F. ferulaeoides with 11 common peaks to a greater extent, and the corresponding compounds are, respectively, 3-methoxy-1,2-propanediol, D-limonene, L-borneol acetate, terpinyl acetate, 1,5,9-undecatriene, 2,6,10-trimethyl, α-cedrene, and a-bergsmotene, β-cedrene, 8-epi-γ-eudesmol, γ-eudesmol, and hinesol, which are aliphatic, aromatic, monoterpene, sesquiterpene, and their oxygenated derivatives [48]. The GC fingerprint of the volatile oil of F. ferulaeoides and Ferula multicolor was established by Luo. Two kinds of GC fingerprints for volatile oil from ferula have twenty common peaks in which the fingerprint similarity was more than 0.9. In addition, Luo also established two kinds of HPLC fingerprints for water extract from ferula, and there were thirteen common peaks in the HPLC fingerprint of F. ferulaeoides while there were twenty-one common peaks in the HPLC fingerprint of Ferula multicolor [49]. In summary, the common peaks of Ferula ferulaeoides are almost identified as a volatile oil, and it is necessary to strengthen the identification of other chemical constituents.

4.3. Content Determination

The determination of the content of Ferulae mainly focused on flavonoids, polysaccharides, and ferulic acid. The best extraction technology for total flavonoids is as follows: 80% ethanol, reflux extraction at 70 °C for 60 min, which could extract 29.45 mg/g of total flavonoids from 1 g of Uygur medicine F. ferulaeoides [10]. Ultrasonic extraction of F. ferulaeoides polysaccharide is better than Soxhlet extraction. The content of polysaccharide was determined by phenol-sulfuric acid colorimetry. The results show that the content of polysaccharide extracted by Soxhlet extraction and ultrasonic extraction is 2.87% and 3.22%, respectively [11]. The best extraction process of ferulic acid was the ratio of material to liquid ratio of 1:40, sodium hydroxide solution of 3%, and an extraction time of 30 min. Under these conditions, the content of ferulic acid from F. ferulaeoides reached 0.2998 mg/g [12]. The determination of coumarin content has also been involved; Zhu et al. established the UPLC method for the determination of DAW22 from F. ferulaeoides of different growth periods in Xinjiang. That indicated that the linear range of DAW22 was 6.21–124.2 ng (r = 10,000) with an average recovery of 99.81% (RSD 2.0%). The content of DAW22 in F. ferulaeoides growing on May 9 was the highest [50]. In general, there are few studies on the content determination of F. ferulaeoides and the research methods are relatively old. Therefore, modern technologies such as liquid chromatography–mass spectrometry should be used to strengthen the quantitative analysis of other chemical components, especially its characteristic components.

5. Prospect: Application of F. ferulaeoides in Food Industry

Firstly, F. ferulaeoides can be used as raw materials for food or food additives for food processing. There have been studies on the processing of ferulic acid into food and as a food additive. For example, some nomads of central Iran use the dried aerial parts of F. assafoetida L. in the preparation of their delicious local food, “Loghri”, which also contains barley, tomato or tomato paste, beans, and other vegetables. In America, different organs of F. assafoetida L., either in fresh or dried form, are used for cooking as even small parts of this plant can give a pungent smell to foodstuffs. It has also found many applications as a condiment and flavoring agent in chocolates, seasonings, and soft drinks [2]. Moreover, it is proved by research that felllloylphenethylami and femloyltymmine could effectively inhibit the increase in acid values, polar substances’ content, and the oxidative degradation of linoleic acid and 1inolenic acid in frying oil [51]. Secondly, the volatile oil and alcohol extract of F. ferulaeoides have a strong bacteriostatic effect, which can be used to make slow-release capsules or preservative agents for plastic wrap applied to food to have a bacteriostatic and preservative effect. Niazmand et al. [52] developed antimicrobial films by incorporating the hydroalcoholic extract of Ferula asafetida leaf and gum in the polymer matrix of LDP and investigated the antimicrobial effect of the films on different microorganisms and the capability of the produced films for extending the shelf life of the dough. The results show that as a bioactive packaging material, LDPE film containing Ferulae leaves and gum extract is promising, which not only improves food safety and quality, but also has good mechanical, thermal, and barrier properties. Valinezhad et al. [53] prepared a kind of composite material which called chitosan Ferula gummosa EO-nanocomposite (CS-FEO). Further, a transparent and flexible CS-FEO biopolymer film was prepared and characterized. The obtained results demonstrate that the prepared CS-FEO nanocomposite could be a potential candidate for food and biomedical applications as it holds the promising capability of proper interactions and advanced features. Finally, F. ferulaeoides can be used as a raw material for functional food development. With the improvement in people’s quality of life and the enhancement in their awareness of health care, people’s consumption of food with health care function has improved significantly. Functional food has gradually opened the market and become the future development trend of the food industry [54]. F. ferulaeoides contains a variety of bioactive ingredients, which is an ideal material for the development of functional food.

6. Conclusions

All in all, as a national medicine, the quantity of research on F. ferulaeoides is relatively small and not deep enough. First, the modern research of F. ferulaeoides mostly focuses on the studies of active ingredients such as sesquiterpenes, volatile oils, coumarins, etc., and less on active ingredients such as phenylpropanoids, phenolic acids, and other steroids. Second, the research on active ingredients mainly stays in the activity screening, mostly focusing on antibacterial, anti-tumor, anti-inflammatory, and insecticidal aspects, and there is a lack of research into its mechanisms. Third, there is a lack of drug safety evaluation in quality control research, and the identification of the fingerprint is insufficient in its depth. The existing reports are almost focused on the volatile oil, there are relatively few content determinations, and the method is more traditional. Fourth, as a kind of medicine and food homologous substance, there is almost no application research in food compared with other Ferula plants. In the future work, we should definitely strengthen the study of other active components of F. ferulaeoides, and the in-depth study of the material basis and mechanism of action. The identification of other chemical components should be added, and the quantitative analysis of other chemical components should be strengthened by using modern technologies such as liquid chromatography–mass spectrometry. In addition, a safety evaluation method for F. ferulaeoides should be established to provide a scientific basis for a comprehensive evaluation of the quality of medicinal materials. Eventually, we should speed up the development and utilization of F. ferulaeoides products, and deeply explore its development and utilization value.